| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs118203975 |
C>T |
Pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
|
rs118203976 |
C>T |
Pathogenic |
Non coding transcript variant, missense variant, coding sequence variant, 3 prime UTR variant |
|
rs118203977 |
A>C,G |
Pathogenic |
Stop gained, coding sequence variant, synonymous variant, non coding transcript variant |
|
rs118203978 |
T>C,G |
Pathogenic, uncertain-significance |
Missense variant, coding sequence variant, non coding transcript variant |
|
rs140948465 |
G>A,T |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs147750747 |
G>A,C |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs150418024 |
C>G,T |
Conflicting-interpretations-of-pathogenicity, pathogenic, uncertain-significance, benign |
Coding sequence variant, missense variant, intron variant, non coding transcript variant |
|
rs200319160 |
C>G,T |
Pathogenic |
Splice donor variant |
|
rs267607235 |
G>A |
Pathogenic, likely-pathogenic |
Coding sequence variant, 3 prime UTR variant, non coding transcript variant, missense variant |
|
rs556661896 |
A>G,T |
Likely-pathogenic |
Intron variant, stop gained, synonymous variant, coding sequence variant, non coding transcript variant |
|
rs558274487 |
C>A,T |
Pathogenic |
Intron variant, stop gained, missense variant, coding sequence variant, non coding transcript variant |
|
rs559155109 |
A>G |
Uncertain-significance, likely-pathogenic |
Non coding transcript variant, coding sequence variant, 3 prime UTR variant, missense variant |
|
rs570989221 |
T>C |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, coding sequence variant |
|
rs587778809 |
A>T |
Pathogenic |
Splice donor variant, intron variant |
|
rs724159970 |
C>A |
Pathogenic |
Stop gained, 3 prime UTR variant, non coding transcript variant, coding sequence variant |
|
rs724159971 |
G>A |
Pathogenic, likely-pathogenic |
Stop gained, 3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, coding sequence variant, downstream transcript variant |
|
rs727502800 |
C>G |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant, intron variant |
|
rs727502801 |
->A |
Pathogenic |
Intron variant |
|
rs749704755 |
C>A,T |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs751696703 |
T>A |
Likely-pathogenic |
Splice acceptor variant, intron variant |
|
rs755011754 |
G>- |
Likely-benign, conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs775699005 |
->A |
Pathogenic |
Coding sequence variant, non coding transcript variant, frameshift variant |
|
rs776253867 |
C>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant, non coding transcript variant, intron variant |
|
rs778875017 |
G>A,T |
Likely-pathogenic |
Non coding transcript variant, stop gained, coding sequence variant, 3 prime UTR variant, missense variant |
|
rs796052742 |
T>C |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, intron variant, missense variant |
|
rs796052752 |
->T |
Pathogenic |
Frameshift variant, coding sequence variant, non coding transcript variant |
|
rs868732642 |
C>A,T |
Likely-pathogenic |
Splice donor variant, intron variant |
|
rs886041806 |
->A |
Pathogenic |
Coding sequence variant, intron variant, non coding transcript variant, frameshift variant |
|
rs1057518388 |
T>C |
Likely-pathogenic |
3 prime UTR variant, splice acceptor variant, non coding transcript variant |
|
rs1314967038 |
C>T |
Pathogenic |
Splice acceptor variant, intron variant |
|
rs1422791271 |
->A |
Likely-pathogenic |
Splice donor variant |
|
rs1439582451 |
C>- |
Likely-pathogenic, pathogenic |
Intron variant, coding sequence variant, non coding transcript variant, frameshift variant |
|
rs1460276679 |
G>- |
Pathogenic |
Intron variant, frameshift variant, coding sequence variant, non coding transcript variant |
|
rs1553946656 |
C>T |
Pathogenic |
Splice donor variant |
|
rs1553950197 |
C>T |
Likely-pathogenic |
Intron variant, splice donor variant, coding sequence variant, missense variant |
|
rs1560747815 |
T>A |
Likely-pathogenic |
Intron variant, splice acceptor variant |
|
rs1560776422 |
C>A |
Pathogenic |
Stop gained, 5 prime UTR variant, non coding transcript variant, splice acceptor variant, coding sequence variant |
|
rs1578794927 |
G>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant, 3 prime UTR variant |
|
rs1578889355 |
AACTGGTGTTGTATACA>- |
Likely-pathogenic |
Non coding transcript variant, coding sequence variant, intron variant, frameshift variant |
|
rs1578912362 |
C>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs1578912759 |
T>C |
Likely-pathogenic |
Splice acceptor variant |
|