| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs61752137 |
C>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
|
rs61752138 |
T>G |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs111286659 |
G>A,T |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Intron variant |
|
rs115760878 |
G>A,C |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, synonymous variant |
|
rs138205085 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, synonymous variant |
|
rs138243167 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, synonymous variant |
|
rs142408719 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, coding sequence variant |
|
rs143571888 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, coding sequence variant |
|
rs144165818 |
T>C |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, coding sequence variant |
|
rs144331955 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, coding sequence variant |
|
rs145690714 |
G>A,T |
Conflicting-interpretations-of-pathogenicity |
Missense variant, non coding transcript variant, coding sequence variant |
|
rs148914171 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, synonymous variant, coding sequence variant |
|
rs149102738 |
G>C |
Likely-benign, conflicting-interpretations-of-pathogenicity, uncertain-significance |
Non coding transcript variant, missense variant, coding sequence variant |
|
rs151312595 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, synonymous variant, coding sequence variant |
|
rs189631769 |
G>A,T |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs376699778 |
C>A,G,T |
Conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs541455903 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, synonymous variant, intron variant |
|
rs747216258 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, non coding transcript variant, synonymous variant |
|
rs748956654 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
|
rs796051881 |
->A |
Pathogenic |
Intron variant, frameshift variant, non coding transcript variant, coding sequence variant |
|
rs886041656 |
GAA>TC |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
|
rs932238098 |
A>G |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, non coding transcript variant, upstream transcript variant, coding sequence variant, genic upstream transcript variant |
|
rs1064793563 |
G>A |
Pathogenic |
Splice acceptor variant |
|
rs1085307998 |
G>A |
Likely-pathogenic |
Intron variant |
|
rs1555176945 |
A>G |
Pathogenic |
Splice acceptor variant |
|
rs1565673352 |
G>T |
Likely-pathogenic, pathogenic |
Stop gained, coding sequence variant, non coding transcript variant |