| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs121908581 |
G>A |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121908582 |
A>G |
Pathogenic |
Coding sequence variant, missense variant |
|
rs137853921 |
A>G |
Conflicting-interpretations-of-pathogenicity, likely-pathogenic |
Coding sequence variant, missense variant |
|
rs143191074 |
A>G |
Benign, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs179363897 |
G>A |
Pathogenic |
Missense variant, coding sequence variant |
|
rs587777828 |
A>G |
Pathogenic |
Intron variant |
|
rs753234582 |
G>C |
Pathogenic |
Splice acceptor variant |
|
rs767221160 |
G>A,T |
Pathogenic |
Coding sequence variant, missense variant, stop gained |
|
rs767822498 |
T>A,C |
Pathogenic |
Initiator codon variant, missense variant |
|
rs772757329 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
|
rs786205636 |
G>A |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs786205637 |
GAA>- |
Likely-pathogenic |
Coding sequence variant, inframe deletion |
|
rs1054138918 |
G>C |
Likely-pathogenic |
Splice acceptor variant |
|
rs1238632042 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs1272140892 |
A>- |
Pathogenic |
Coding sequence variant, frameshift variant |
|
rs1466289570 |
G>A,T |
Likely-pathogenic |
Splice acceptor variant |
|
rs1477098739 |
A>G |
Pathogenic |
Splice acceptor variant |
|
rs1553529427 |
->T |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1559121920 |
A>G |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1559122157 |
T>C |
Pathogenic |
Splice donor variant |
|
rs1559122277 |
G>T |
Likely-pathogenic |
Splice donor variant |
|
rs1574339529 |
T>A |
Pathogenic |
Coding sequence variant, stop gained |