| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs121918525 |
G>A |
Pathogenic, uncertain-significance |
Coding sequence variant, missense variant |
|
rs121918526 |
C>T |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant |
|
rs121918527 |
G>A |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant |
|
rs140734968 |
G>C |
Conflicting-interpretations-of-pathogenicity, benign |
Coding sequence variant, synonymous variant |
|
rs142126065 |
C>T |
Conflicting-interpretations-of-pathogenicity, benign |
Coding sequence variant, synonymous variant |
|
rs144449744 |
G>A |
Conflicting-interpretations-of-pathogenicity, likely-benign |
Synonymous variant, coding sequence variant |
|
rs782393002 |
A>C,G |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs863224879 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs886041876 |
G>A |
Pathogenic-likely-pathogenic, pathogenic |
Missense variant, coding sequence variant |
|
rs1057517893 |
A>G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs1057518704 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1057520538 |
G>A |
Uncertain-significance, pathogenic |
Missense variant, coding sequence variant |
|
rs1057521722 |
C>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1057521730 |
C>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1057521791 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1057521796 |
T>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1057524560 |
A>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1064793631 |
A>G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs1325394060 |
C>G,T |
Likely-pathogenic |
Synonymous variant, missense variant, coding sequence variant |
|
rs1556909287 |
C>G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs1556909335 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556910184 |
C>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556910261 |
C>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556911750 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556912828 |
G>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556913180 |
T>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556913258 |
G>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556913268 |
T>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556914274 |
G>A |
Uncertain-significance, likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556927963 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556928966 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556955128 |
A>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1556978515 |
T>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1557006873 |
A>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1557006903 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1557024919 |
C>G |
Pathogenic |
Splice donor variant |
|
rs1557036757 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1557036768 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs1569398624 |
C>A |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs1569399945 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1569509136 |
T>C |
Pathogenic, likely-pathogenic |
Splice acceptor variant |
|
rs1602738933 |
AGTTGAAGCTGTTGAGAAAAGTCAAACACTGG>- |
Likely-pathogenic |
Coding sequence variant, splice acceptor variant, intron variant |