| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs28936415 |
G>A |
Pathogenic, likely-pathogenic |
Missense variant, coding sequence variant |
|
rs80338700 |
C>G,T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs80338701 |
C>A,T |
Pathogenic |
Synonymous variant, coding sequence variant, missense variant |
|
rs80338702 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs80338703 |
G>A |
Pathogenic-likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
|
rs80338704 |
A>G |
Pathogenic-likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
|
rs104894525 |
G>A,T |
Pathogenic-likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
|
rs104894526 |
C>T |
Pathogenic-likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
|
rs104894527 |
G>T |
Pathogenic |
Intron variant, coding sequence variant, missense variant |
|
rs104894530 |
G>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs104894533 |
T>G |
Pathogenic |
5 prime UTR variant, coding sequence variant, missense variant |
|
rs104894534 |
T>C |
Likely-pathogenic |
5 prime UTR variant, coding sequence variant, missense variant |
|
rs139716296 |
T>C,G |
Pathogenic |
Intron variant, splice donor variant |
|
rs141498002 |
G>A,T |
Conflicting-interpretations-of-pathogenicity, pathogenic |
Coding sequence variant, missense variant |
|
rs146990448 |
C>G,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
|
rs148032587 |
G>A |
Pathogenic-likely-pathogenic, pathogenic |
Coding sequence variant, missense variant |
|
rs149530060 |
C>G,T |
Pathogenic |
Coding sequence variant, 5 prime UTR variant, stop gained, missense variant |
|
rs149849259 |
G>A,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
|
rs150577656 |
T>A,C,G |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs150719105 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs190521996 |
T>C |
Pathogenic-likely-pathogenic, pathogenic |
Missense variant, coding sequence variant |
|
rs191295403 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
|
rs199562225 |
C>T |
Pathogenic-likely-pathogenic |
Stop gained, coding sequence variant |
|
rs200503569 |
C>T |
Likely-pathogenic, pathogenic-likely-pathogenic |
Missense variant, coding sequence variant |
|
rs201556985 |
C>G |
Likely-benign, uncertain-significance, conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant, 5 prime UTR variant |
|
rs367852554 |
G>A |
Likely-pathogenic |
Intron variant |
|
rs368582085 |
T>C |
Conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant |
|
rs376754460 |
G>A,C,T |
Likely-pathogenic |
Missense variant, 5 prime UTR variant, coding sequence variant |
|
rs398123309 |
G>A,C |
Pathogenic-likely-pathogenic, pathogenic |
Missense variant, coding sequence variant |
|
rs398123312 |
TA>GC |
Pathogenic |
Missense variant, 5 prime UTR variant, coding sequence variant |
|
rs532870929 |
T>C |
Pathogenic-likely-pathogenic |
Missense variant, coding sequence variant |
|
rs746610168 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs749720760 |
T>C |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
Missense variant, 5 prime UTR variant, coding sequence variant |
|
rs753632453 |
A>G,T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs754407762 |
C>G,T |
Pathogenic |
Missense variant, stop gained, coding sequence variant |
|
rs755008774 |
A>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs757394782 |
G>C |
Pathogenic |
Splice acceptor variant |
|
rs764353860 |
C>T |
Pathogenic-likely-pathogenic |
Coding sequence variant, 5 prime UTR variant, stop gained |
|
rs765433263 |
C>A,T |
Uncertain-significance, likely-pathogenic |
Missense variant, coding sequence variant |
|
rs769648248 |
C>G,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, intron variant, missense variant |
|
rs770458492 |
C>G |
Pathogenic |
Coding sequence variant, missense variant |
|
rs771240150 |
AA>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs780581250 |
T>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs940938678 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1057516323 |
->A |
Pathogenic-likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1057516372 |
A>G |
Likely-pathogenic |
Splice acceptor variant |
|
rs1057516757 |
->G |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1057516815 |
A>- |
Likely-pathogenic |
Intron variant, frameshift variant, coding sequence variant |
|
rs1057516886 |
G>A |
Likely-pathogenic |
Stop gained, coding sequence variant |
|
rs1057517110 |
T>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1057517117 |
G>A |
Likely-pathogenic |
Splice donor variant |
|
rs1057517183 |
G>A |
Likely-pathogenic |
Splice donor variant |
|
rs1057520708 |
C>T |
Pathogenic |
Stop gained, 5 prime UTR variant, coding sequence variant |
|
rs1060499598 |
G>A |
Pathogenic-likely-pathogenic |
Intron variant, splice donor variant |
|
rs1166138838 |
G>C,T |
Likely-pathogenic |
Intron variant, splice acceptor variant |
|
rs1258107584 |
C>T |
Likely-pathogenic |
Intron variant |
|
rs1274794195 |
GAAA>- |
Likely-pathogenic |
Coding sequence variant, splice acceptor variant |
|
rs1339004837 |
T>- |
Likely-pathogenic |
Coding sequence variant, intron variant, frameshift variant |
|
rs1555448897 |
A>T |
Likely-pathogenic |
Splice acceptor variant |
|
rs1555448899 |
T>A |
Likely-pathogenic |
Stop gained, 5 prime UTR variant, coding sequence variant |
|
rs1555448922 |
T>G |
Likely-pathogenic |
Splice donor variant |
|
rs1555449314 |
G>- |
Pathogenic, likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1555449603 |
A>C |
Likely-pathogenic |
Splice acceptor variant |
|
rs1555449604 |
G>C |
Likely-pathogenic |
Splice acceptor variant |
|
rs1555449607 |
C>- |
Pathogenic, likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1555449617 |
C>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1555449780 |
A>G |
Likely-pathogenic |
Splice acceptor variant |
|
rs1596489887 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant |