| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs121434611 |
C>T |
Pathogenic |
Coding sequence variant, non coding transcript variant, stop gained, genic downstream transcript variant |
|
rs121434612 |
C>T |
Pathogenic |
Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript variant |
|
rs121434613 |
C>A |
Pathogenic |
Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript variant |
|
rs121434614 |
G>C |
Pathogenic |
Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript variant |
|
rs200474454 |
A>G |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Non coding transcript variant, coding sequence variant, missense variant, genic downstream transcript variant |
|
rs780775497 |
C>A,T |
Likely-pathogenic |
Genic downstream transcript variant, non coding transcript variant, coding sequence variant, stop gained, synonymous variant |
|
rs1556298136 |
G>A |
Likely-pathogenic |
Genic downstream transcript variant, non coding transcript variant, missense variant, coding sequence variant |
|
rs1556298855 |
T>G |
Likely-pathogenic |
Genic downstream transcript variant, non coding transcript variant, missense variant, coding sequence variant |
|
rs1569398769 |
A>G |
Pathogenic |
Genic downstream transcript variant, intron variant |
|
rs1569398792 |
G>A |
Likely-pathogenic |
Genic downstream transcript variant, intron variant |
|
rs1569459580 |
G>A |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant, genic downstream transcript variant |
|
rs1603373827 |
G>C |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant, genic downstream transcript variant |
|
rs1603377813 |
G>A |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant, genic downstream transcript variant |
|
rs1603378331 |
T>A |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant, genic downstream transcript variant |
|