| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs144106353 |
T>C |
Conflicting-interpretations-of-pathogenicity |
5 prime UTR variant, genic upstream transcript variant, coding sequence variant, non coding transcript variant, synonymous variant |
|
rs148448660 |
G>A |
Conflicting-interpretations-of-pathogenicity |
5 prime UTR variant, missense variant, genic upstream transcript variant, non coding transcript variant, coding sequence variant |
|
rs397509359 |
C>A,T |
Pathogenic |
Non coding transcript variant, genic downstream transcript variant |
|
rs767354861 |
C>T |
Likely-pathogenic |
Coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs864321627 |
T>C |
Pathogenic |
Genic upstream transcript variant, genic downstream transcript variant, non coding transcript variant, missense variant, coding sequence variant |
|
rs864321628 |
T>C |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant, genic upstream transcript variant |
|
rs864321629 |
C>T |
Pathogenic |
Genic upstream transcript variant, genic downstream transcript variant, non coding transcript variant, missense variant, coding sequence variant |
|
rs864321630 |
C>T |
Likely-pathogenic, pathogenic |
Missense variant, non coding transcript variant, coding sequence variant, genic upstream transcript variant |
|
rs864321631 |
G>C |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant, genic upstream transcript variant |
|
rs1057518019 |
C>T |
Likely-pathogenic |
Missense variant, genic upstream transcript variant, coding sequence variant, non coding transcript variant |
|
rs1064793874 |
A>G |
Likely-pathogenic |
Missense variant, genic downstream transcript variant, genic upstream transcript variant, coding sequence variant, non coding transcript variant |
|
rs1131691982 |
G>A |
Likely-pathogenic |
Missense variant, genic downstream transcript variant, genic upstream transcript variant, coding sequence variant, non coding transcript variant |
|
rs1555980523 |
C>T |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, missense variant, genic downstream transcript variant, coding sequence variant |
|
rs1555980614 |
T>C |
Likely-pathogenic |
Non coding transcript variant, genic upstream transcript variant, missense variant, genic downstream transcript variant, coding sequence variant |
|
rs1569301036 |
C>T |
Pathogenic |
Genic downstream transcript variant, coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602481623 |
A>G |
Likely-pathogenic |
Coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602489684 |
G>A |
Likely-pathogenic |
Coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602506017 |
C>T |
Likely-pathogenic |
Coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602520317 |
C>T |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, genic upstream transcript variant, 3 prime UTR variant, missense variant |
|
rs1602538353 |
C>T |
Likely-pathogenic |
Genic downstream transcript variant, coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602572645 |
A>G,T |
Likely-pathogenic, uncertain-significance |
Genic downstream transcript variant, coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602624914 |
A>C |
Likely-pathogenic |
Genic downstream transcript variant, coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|
rs1602624950 |
C>T |
Likely-pathogenic |
Genic downstream transcript variant, coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant |
|