SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs372031019 |
G>A,C,T |
Likely-pathogenic |
Coding sequence variant, synonymous variant, missense variant |
rs387907345 |
C>T |
Likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
rs387907347 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
rs387907348 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
rs387907349 |
G>A |
Likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
rs387907350 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
rs747559032 |
G>A |
Pathogenic |
Coding sequence variant, missense variant |
rs751173836 |
C>A,T |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs867564562 |
G>T |
Likely-pathogenic, uncertain-significance |
Coding sequence variant, missense variant |
rs1555343284 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
rs1594751659 |
A>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594751825 |
C>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594751831 |
T>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594755688 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594756590 |
A>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594758038 |
->CTCCATGGCCCC |
Likely-pathogenic |
Inframe indel, coding sequence variant |
rs1594758046 |
T>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594760036 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594760140 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594768463 |
T>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594771155 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594771224 |
T>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594771236 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594771270 |
T>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs1594773549 |
G>C |
Uncertain-significance, likely-pathogenic |
Missense variant, coding sequence variant |