| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs58606740 |
G>A |
Pathogenic |
Splice donor variant |
|
rs121918039 |
G>A |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant, intron variant |
|
rs121918040 |
C>T |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant |
|
rs121918041 |
C>T |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant, intron variant |
|
rs121918042 |
C>T |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant |
|
rs121918043 |
A>T |
Pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
|
rs145343957 |
G>A |
Benign, conflicting-interpretations-of-pathogenicity |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs145877597 |
G>A,T |
Uncertain-significance, likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs200001068 |
C>A,G,T |
Pathogenic |
Stop gained, synonymous variant, non coding transcript variant, coding sequence variant, missense variant |
|
rs369678636 |
C>T |
Pathogenic |
Coding sequence variant, stop gained, non coding transcript variant |
|
rs398122932 |
->AGG |
Pathogenic |
Coding sequence variant, non coding transcript variant, genic upstream transcript variant, inframe insertion |
|
rs398123307 |
C>A |
Likely-pathogenic |
Coding sequence variant, missense variant, intron variant |
|
rs398123308 |
G>A |
Pathogenic |
Genic upstream transcript variant, splice donor variant |
|
rs555242193 |
C>A,T |
Pathogenic, benign |
Coding sequence variant, non coding transcript variant, synonymous variant, stop gained |
|
rs749004212 |
C>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs752024467 |
G>A |
Likely-pathogenic |
Splice donor variant |
|
rs755226061 |
C>A,G,T |
Pathogenic |
Missense variant, synonymous variant, coding sequence variant, stop gained, non coding transcript variant |
|
rs757757289 |
A>-,AA |
Pathogenic |
Coding sequence variant, frameshift variant, non coding transcript variant |
|
rs778235410 |
C>G,T |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant, missense variant |
|
rs778707203 |
G>A,C,T |
Likely-pathogenic |
Stop gained, coding sequence variant, non coding transcript variant, missense variant |
|
rs778896252 |
AAACTT>- |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, inframe deletion |
|
rs780351760 |
C>A,T |
Likely-pathogenic |
Non coding transcript variant, stop gained, coding sequence variant, 5 prime UTR variant, synonymous variant |
|
rs886041114 |
G>A,T |
Uncertain-significance, likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant, synonymous variant |
|
rs1057518797 |
CCCGGGCA>TAGGACG |
Pathogenic |
Genic upstream transcript variant, coding sequence variant, non coding transcript variant, frameshift variant |
|
rs1057518906 |
C>T |
Pathogenic |
Genic upstream transcript variant, coding sequence variant, non coding transcript variant, stop gained |
|
rs1057518969 |
CT>- |
Pathogenic |
5 prime UTR variant, coding sequence variant, non coding transcript variant, frameshift variant |
|
rs1060503526 |
C>T |
Pathogenic |
Coding sequence variant, non coding transcript variant, stop gained |
|
rs1131692280 |
G>A |
Pathogenic |
Splice donor variant, intron variant |
|
rs1135401753 |
C>G |
Pathogenic |
Coding sequence variant, non coding transcript variant, stop gained |
|
rs1187336837 |
C>-,CC |
Pathogenic |
Genic upstream transcript variant, frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1232369409 |
G>- |
Pathogenic |
Frameshift variant, genic upstream transcript variant, non coding transcript variant, coding sequence variant |
|
rs1255557802 |
G>A,C,T |
Likely-pathogenic |
Non coding transcript variant, stop gained, coding sequence variant, missense variant |
|
rs1276594505 |
C>G,T |
Pathogenic |
Coding sequence variant, stop gained, missense variant, non coding transcript variant |
|
rs1302726543 |
C>T |
Pathogenic |
Coding sequence variant, non coding transcript variant, upstream transcript variant, genic upstream transcript variant, stop gained |
|
rs1324209174 |
C>T |
Pathogenic |
Intron variant, non coding transcript variant, coding sequence variant, stop gained |
|
rs1355372474 |
C>T |
Likely-pathogenic |
Stop gained, genic upstream transcript variant, non coding transcript variant, coding sequence variant |
|
rs1371793191 |
->C,CCC |
Pathogenic |
Frameshift variant, non coding transcript variant, genic upstream transcript variant, coding sequence variant, inframe insertion |
|
rs1391596181 |
T>A,C |
Pathogenic |
Missense variant, non coding transcript variant, stop gained, coding sequence variant |
|
rs1553923513 |
GGCCCGCCGTGCCCCAGCCCAG>- |
Likely-pathogenic, pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant, genic upstream transcript variant |
|
rs1553924158 |
G>A |
Pathogenic |
Coding sequence variant, non coding transcript variant, genic upstream transcript variant, upstream transcript variant, stop gained |
|
rs1553924173 |
C>- |
Pathogenic |
Coding sequence variant, non coding transcript variant, genic upstream transcript variant, upstream transcript variant, frameshift variant |
|
rs1553924174 |
->C |
Likely-pathogenic |
Coding sequence variant, 5 prime UTR variant, non coding transcript variant, genic upstream transcript variant, frameshift variant |
|
rs1553925453 |
C>T |
Likely-pathogenic, pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
|
rs1553925459 |
G>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1553925467 |
G>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1553925470 |
AAGT>- |
Uncertain-significance, pathogenic |
Intron variant, splice donor variant |
|
rs1553926509 |
TA>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1553926529 |
GTTCAACA>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1553926905 |
C>T |
Pathogenic |
Non coding transcript variant, stop gained, coding sequence variant |
|
rs1553926929 |
G>A |
Likely-pathogenic, pathogenic |
Intron variant |
|
rs1553927080 |
G>A |
Likely-pathogenic |
Intron variant, splice donor variant |
|
rs1553927436 |
GA>- |
Likely-pathogenic |
Non coding transcript variant, splice acceptor variant, coding sequence variant |
|
rs1553927783 |
G>A |
Likely-pathogenic |
Splice donor variant |
|
rs1553927823 |
TACG>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1553928728 |
G>A |
Pathogenic |
Splice acceptor variant |
|
rs1553928730 |
C>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1560592253 |
G>- |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant, genic upstream transcript variant |
|
rs1560597874 |
G>T |
Pathogenic |
Upstream transcript variant, splice acceptor variant, genic upstream transcript variant |
|
rs1560598042 |
->C |
Pathogenic |
Genic upstream transcript variant, 5 prime UTR variant, frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1560608729 |
C>AGA |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1560617356 |
TCAA>- |
Likely-pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1560620277 |
TAACAGGACC>AACAGG |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1560621750 |
AC>T |
Pathogenic |
Intron variant, frameshift variant, coding sequence variant |
|
rs1560626499 |
A>G |
Pathogenic |
Splice acceptor variant |
|
rs1560626561 |
->AT |
Likely-pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1560628245 |
->T |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1560632930 |
G>- |
Pathogenic |
Stop gained, non coding transcript variant, coding sequence variant |
|
rs1578111209 |
CTCTGCGAGCAGCGGGGCCTGGAGATCGAGATGCAGCGCATCCGGCAGGCGGCCGCGCGGGACCCCCCGGCCGGA>GCGGG |
Pathogenic |
Non coding transcript variant, coding sequence variant, genic upstream transcript variant, frameshift variant |
|
rs1578111345 |
G>A |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained, genic upstream transcript variant |
|
rs1578111378 |
G>T |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, stop gained, genic upstream transcript variant |
|
rs1578111620 |
A>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, genic upstream transcript variant, frameshift variant |
|
rs1578111741 |
AG>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, genic upstream transcript variant, frameshift variant |
|
rs1578111778 |
G>C |
Pathogenic |
Genic upstream transcript variant, splice donor variant |
|
rs1578118330 |
AA>- |
Pathogenic |
Non coding transcript variant, genic upstream transcript variant, coding sequence variant, frameshift variant, upstream transcript variant |
|
rs1578118371 |
C>- |
Likely-pathogenic |
Non coding transcript variant, 5 prime UTR variant, genic upstream transcript variant, coding sequence variant, frameshift variant |
|
rs1578129049 |
C>G |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained, 5 prime UTR variant |
|
rs1578130536 |
G>C |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
|
rs1578130597 |
->T |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578130676 |
C>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs1578133684 |
C>AA |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, intron variant, frameshift variant |
|
rs1578135823 |
A>- |
Pathogenic |
Splice acceptor variant |
|
rs1578135829 |
T>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578135842 |
G>A |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
|
rs1578135870 |
G>A |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs1578139269 |
->A |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578141765 |
->A |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578142941 |
GTATG>- |
Pathogenic |
Coding sequence variant, intron variant, splice donor variant |
|
rs1578144873 |
->A |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs1578144898 |
TC>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578147448 |
A>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs1578147458 |
->GCCATACTGG |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578148821 |
G>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs1578153553 |
->A |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs1578153598 |
T>C |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
|