| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs122461162 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
|
rs139299794 |
C>T |
Conflicting-interpretations-of-pathogenicity, benign |
Coding sequence variant, synonymous variant, 5 prime UTR variant |
|
rs151178361 |
G>A |
Conflicting-interpretations-of-pathogenicity, likely-benign |
Synonymous variant, coding sequence variant |
|
rs190788663 |
C>T |
Conflicting-interpretations-of-pathogenicity |
3 prime UTR variant |
|
rs398122849 |
GGTGCTGCT>- |
Pathogenic |
Inframe deletion, coding sequence variant |
|
rs398123003 |
G>T |
Pathogenic |
Stop gained, coding sequence variant |
|
rs398124224 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
|
rs587784398 |
G>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs587784399 |
T>G |
Pathogenic |
Stop gained, coding sequence variant |
|
rs730882187 |
AA>CC |
Pathogenic |
Intron variant |
|
rs730882188 |
AT>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs782108464 |
G>A,C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs782296172 |
C>A,G |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant, missense variant |
|
rs796053283 |
G>A |
Pathogenic |
Splice donor variant |
|
rs796053284 |
G>A |
Likely-pathogenic |
Intron variant |
|
rs796053290 |
TTTTA>- |
Uncertain-significance, likely-pathogenic, pathogenic |
Intron variant |
|
rs796053291 |
->G |
Pathogenic |
Splice acceptor variant, coding sequence variant |
|
rs796053293 |
->C |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs796053297 |
CA>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs797044508 |
G>A |
Pathogenic |
Splice acceptor variant |
|
rs886037619 |
AAAGTG>- |
Pathogenic |
Inframe deletion, coding sequence variant |
|
rs1006154022 |
T>G |
Likely-pathogenic |
Missense variant, initiator codon variant, intron variant |
|
rs1057519394 |
T>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs1064793575 |
GT>- |
Likely-pathogenic, pathogenic |
Frameshift variant, coding sequence variant |
|
rs1064795183 |
GA>- |
Pathogenic |
Coding sequence variant, splice acceptor variant |
|
rs1556617455 |
G>A |
Pathogenic, likely-pathogenic |
Splice donor variant |
|
rs1556620027 |
TATTTAC>GTCTTGGGAAGAGCT |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs1569525357 |
G>A |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs1569525894 |
TCTTCCTTAACCACCGC>- |
Likely-pathogenic |
Intron variant |
|
rs1603198063 |
AT>- |
Pathogenic |
Coding sequence variant, frameshift variant |
|
rs1603198937 |
G>A |
Pathogenic |
Splice donor variant |
|
rs1603201557 |
CTT>- |
Likely-pathogenic |
Coding sequence variant, inframe deletion |
|
rs1603201598 |
->T |
Likely-pathogenic |
Splice donor variant |
|
rs1603215383 |
G>A |
Pathogenic |
Splice acceptor variant |
|
rs1603219805 |
AAGGA>- |
Pathogenic |
Coding sequence variant, frameshift variant |