| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
| rs34965084 |
G>A |
Benign-likely-benign, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, genic downstream transcript variant, 3 prime UTR variant, missense variant |
| rs398123036 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
| rs536853368 |
A>C,G,T |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs757204777 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs770440975 |
G>A |
Likely-pathogenic |
Coding sequence variant, missense variant |
| rs774649299 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
| rs776171893 |
A>G,T |
Pathogenic |
Coding sequence variant, missense variant |
| rs786205560 |
A>C |
Uncertain-significance, likely-pathogenic |
Missense variant, coding sequence variant |
| rs864309642 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
| rs864309643 |
G>A |
Pathogenic |
Missense variant, coding sequence variant |
| rs879255408 |
C>T |
Likely-pathogenic |
Stop gained, coding sequence variant |
| rs1163473923 |
C>T |
Likely-pathogenic |
Stop gained, coding sequence variant |
| rs1575240334 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs1575308774 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |