| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs41280332 |
A>G |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs145268448 |
C>A |
Conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs192669225 |
G>A |
Likely-pathogenic |
Missense variant, intron variant, coding sequence variant, non coding transcript variant |
|
rs587777391 |
G>- |
Pathogenic |
Coding sequence variant, frameshift variant, non coding transcript variant, intron variant |
|
rs587777392 |
G>C |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
|
rs587777393 |
C>A |
Pathogenic |
Stop gained, coding sequence variant, non coding transcript variant |
|
rs587777394 |
G>T |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
|
rs587777395 |
G>A,T |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
|
rs587777769 |
T>- |
Pathogenic |
Coding sequence variant, frameshift variant, 5 prime UTR variant, intron variant |
|
rs746332433 |
G>C,T |
Uncertain-significance, likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
|
rs753591864 |
G>A,T |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, stop gained, missense variant |
|
rs760433806 |
C>T |
Likely-pathogenic |
Stop gained, synonymous variant, coding sequence variant, non coding transcript variant |
|
rs869312928 |
A>G |
Likely-pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
|
rs875989844 |
C>G |
Pathogenic |
Coding sequence variant, stop gained, non coding transcript variant |
|
rs1131691563 |
T>G |
Pathogenic |
Splice donor variant |
|
rs1131691574 |
A>G |
Likely-pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
|
rs1156299044 |
TG>- |
Likely-pathogenic |
5 prime UTR variant, coding sequence variant, frameshift variant, intron variant |
|
rs1553230375 |
T>G |
Pathogenic |
Non coding transcript variant, coding sequence variant, missense variant |
|