| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
| rs182956712 |
C>G |
Conflicting-interpretations-of-pathogenicity |
Intron variant |
| rs200488568 |
T>C |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant |
| rs201399007 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
| rs201985055 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
| rs202049257 |
G>A,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
| rs374299843 |
G>A,C |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, coding sequence variant |
| rs377428323 |
C>A,T |
Likely-benign, conflicting-interpretations-of-pathogenicity |
Intron variant |
| rs377462059 |
G>A,C |
Conflicting-interpretations-of-pathogenicity |
Intron variant |
| rs587776986 |
T>C |
Pathogenic |
Coding sequence variant, missense variant |
| rs690016543 |
C>T |
Pathogenic, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
| rs1009209509 |
C>T |
Likely-pathogenic |
Splice donor variant |
| rs1057519117 |
C>A |
Likely-pathogenic |
Splice acceptor variant |
| rs1404020990 |
A>C |
Pathogenic |
Coding sequence variant, missense variant |
| rs1569512576 |
CC>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
| rs1569513495 |
C>A |
Likely-pathogenic |
Coding sequence variant, stop gained |
| rs1603430221 |
CA>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |