| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs104893863 |
C>T |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs104893864 |
A>C |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs104893865 |
A>G |
Pathogenic |
Intron variant, missense variant, non coding transcript variant, coding sequence variant |
|
rs104893866 |
T>C |
Pathogenic |
Intron variant, missense variant, coding sequence variant |
|
rs104893867 |
C>T |
Pathogenic |
Stop gained, non coding transcript variant, coding sequence variant |
|
rs750201480 |
G>A |
Likely-pathogenic |
Missense variant, intron variant, coding sequence variant |
|
rs750513275 |
A>C,G |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs762772317 |
C>A,T |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
|
rs779997983 |
G>A |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant |
|
rs1034528249 |
T>A,C |
Pathogenic |
Non coding transcript variant, initiator codon variant, missense variant |
|
rs1171544975 |
G>C |
Pathogenic |
Coding sequence variant, non coding transcript variant, stop gained |
|
rs1407920390 |
G>A |
Pathogenic |
Coding sequence variant, non coding transcript variant, missense variant |
|
rs1577184852 |
T>C |
Likely-pathogenic |
Splice acceptor variant |
|
rs1577191558 |
G>- |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
|
rs1577195951 |
G>- |
Pathogenic |
Intron variant, frameshift variant, non coding transcript variant, coding sequence variant |
|