| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs34667348 |
C>A,T |
Uncertain-significance, pathogenic-likely-pathogenic, conflicting-interpretations-of-pathogenicity |
Stop gained, missense variant, coding sequence variant |
|
rs61494991 |
T>C |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, coding sequence variant |
|
rs111734407 |
T>A,C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121918021 |
T>A,G |
Pathogenic |
Coding sequence variant, stop gained |
|
rs139738333 |
A>G |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Coding sequence variant, missense variant |
|
rs142381554 |
A>G |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs145166656 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
|
rs149244943 |
C>A,T |
Pathogenic |
Coding sequence variant, stop gained, missense variant |
|
rs199948078 |
G>A,T |
Pathogenic |
Stop gained, missense variant, coding sequence variant |
|
rs201995780 |
G>T |
Likely-benign, conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs371296953 |
G>A,T |
Likely-pathogenic |
Stop gained, missense variant, coding sequence variant |
|
rs748262135 |
C>T |
Likely-pathogenic |
Stop gained, coding sequence variant |
|
rs758004953 |
C>T |
Uncertain-significance, pathogenic |
Coding sequence variant, stop gained |
|
rs797044442 |
A>G |
Pathogenic |
Splice acceptor variant |
|
rs1273669177 |
C>T |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs1322527832 |
A>- |
Pathogenic |
Coding sequence variant, frameshift variant |