| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs121917882 |
C>A,T |
Pathogenic |
5 prime UTR variant, coding sequence variant, missense variant |
|
rs121917884 |
T>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs137852957 |
T>C |
Pathogenic |
5 prime UTR variant, coding sequence variant, missense variant |
|
rs137852958 |
C>A,G |
Pathogenic |
Stop gained, coding sequence variant, missense variant |
|
rs138363524 |
G>A,C |
Conflicting-interpretations-of-pathogenicity, uncertain-significance, likely-benign |
Coding sequence variant, synonymous variant |
|
rs141957107 |
C>T |
Pathogenic |
Splice donor variant |
|
rs142166552 |
G>A |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Coding sequence variant, missense variant |
|
rs145288025 |
C>T |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Missense variant, coding sequence variant |
|
rs145804755 |
T>C |
Benign-likely-benign, conflicting-interpretations-of-pathogenicity, uncertain-significance |
Missense variant, coding sequence variant |
|
rs145999922 |
A>G |
Pathogenic-likely-pathogenic |
Missense variant, coding sequence variant |
|
rs147205930 |
T>C |
Likely-benign, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
|
rs147502239 |
C>G,T |
Conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant |
|
rs148144444 |
C>G,T |
Benign-likely-benign, conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant |
|
rs149806390 |
G>C |
Conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant |
|
rs200542114 |
T>A,C |
Pathogenic |
Intron variant |
|
rs367737262 |
T>A,C |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Intron variant |
|
rs368364131 |
G>C |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs563607795 |
A>C,G |
Pathogenic, uncertain-significance |
Missense variant, coding sequence variant |
|
rs713993048 |
G>T |
Pathogenic |
5 prime UTR variant, stop gained, coding sequence variant |
|
rs759807393 |
T>C,G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs763130915 |
GAC>- |
Likely-pathogenic |
Inframe deletion, coding sequence variant |
|
rs773140674 |
A>-,AA |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs773971505 |
A>G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs775835429 |
->TC |
Pathogenic |
Frameshift variant, coding sequence variant, 5 prime UTR variant |
|
rs786205213 |
->A |
Pathogenic |
Frameshift variant, coding sequence variant, 5 prime UTR variant |
|
rs863224204 |
G>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs980641322 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs1064795112 |
T>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1085307963 |
T>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1131691615 |
G>A |
Pathogenic |
Missense variant, coding sequence variant |
|
rs1131691902 |
C>A,T |
Likely-pathogenic |
5 prime UTR variant, missense variant, coding sequence variant, stop gained |
|
rs1282844765 |
G>A |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1553568249 |
TAC>- |
Pathogenic |
Coding sequence variant, inframe deletion |
|
rs1553571227 |
A>G |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1553571813 |
A>G |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1559247315 |
->A |
Pathogenic |
Coding sequence variant, frameshift variant |
|
rs1559250774 |
G>T |
Pathogenic |
Coding sequence variant, stop gained |
|
rs1559252723 |
T>- |
Likely-pathogenic |
Coding sequence variant, 5 prime UTR variant, frameshift variant |
|
rs1574558558 |
GGCGCCTTGTAATCCCACAGGATTTGAACAT>- |
Pathogenic |
Coding sequence variant, frameshift variant |