| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs5036 |
T>C |
Pathogenic, benign, likely-benign |
Coding sequence variant, missense variant, 5 prime UTR variant |
|
rs2285644 |
G>A,T |
Pathogenic, benign, likely-benign |
Coding sequence variant, genic downstream transcript variant, downstream transcript variant, missense variant |
|
rs13306787 |
C>A,T |
Pathogenic, uncertain-significance |
Stop gained, missense variant, coding sequence variant |
|
rs28929480 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs28931583 |
G>A,C,T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs28931584 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs28931585 |
G>A,T |
Pathogenic |
Genic downstream transcript variant, downstream transcript variant, coding sequence variant, synonymous variant, missense variant |
|
rs45562031 |
C>T |
Likely-pathogenic, likely-benign, uncertain-significance |
5 prime UTR variant, missense variant, coding sequence variant |
|
rs56361140 |
G>A,C,T |
Pathogenic |
Stop gained, missense variant, coding sequence variant, synonymous variant |
|
rs75731670 |
C>G,T |
Affects |
Missense variant, coding sequence variant |
|
rs121912741 |
C>T |
Pathogenic |
3 prime UTR variant, coding sequence variant, missense variant |
|
rs121912742 |
G>A |
Pathogenic |
Coding sequence variant, stop gained |
|
rs121912743 |
C>G,T |
Affects |
Coding sequence variant, missense variant |
|
rs121912744 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121912745 |
G>A,T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121912746 |
G>A |
Pathogenic |
Coding sequence variant, intron variant, missense variant |
|
rs121912748 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121912749 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121912750 |
T>C |
Pathogenic |
Missense variant, coding sequence variant, downstream transcript variant, genic downstream transcript variant |
|
rs121912751 |
G>T |
Pathogenic, uncertain-significance |
Missense variant, coding sequence variant, downstream transcript variant, genic downstream transcript variant |
|
rs121912752 |
ACC>- |
Pathogenic |
Coding sequence variant, downstream transcript variant, inframe deletion, genic downstream transcript variant |
|
rs121912753 |
A>G |
Pathogenic |
3 prime UTR variant, coding sequence variant, missense variant |
|
rs121912754 |
C>G,T |
Pathogenic |
Coding sequence variant, intron variant, missense variant |
|
rs121912755 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs121912756 |
C>T |
Affects |
Coding sequence variant, missense variant |
|
rs121912757 |
C>T |
Pathogenic, uncertain-significance |
Coding sequence variant, missense variant |
|
rs121912758 |
G>A,T |
Pathogenic |
Coding sequence variant, synonymous variant, missense variant |
|
rs121912759 |
G>A |
Pathogenic, uncertain-significance |
Missense variant, coding sequence variant, downstream transcript variant, genic downstream transcript variant |
|
rs147390654 |
C>A,T |
Conflicting-interpretations-of-pathogenicity, not-provided |
Missense variant, coding sequence variant |
|
rs373916826 |
G>A,T |
Pathogenic |
Synonymous variant, coding sequence variant, missense variant |
|
rs387906565 |
C>T |
Pathogenic |
Upstream transcript variant, genic upstream transcript variant, 5 prime UTR variant |
|
rs387906566 |
->CATCTGGGTG |
Pathogenic |
Genic downstream transcript variant, downstream transcript variant, coding sequence variant, frameshift variant |
|
rs750930293 |
G>A,T |
Pathogenic |
Coding sequence variant, stop gained, synonymous variant |
|
rs769664228 |
GGCAGCCAGGACCTGGGGGCTGAATGC>- |
Pathogenic, protective |
Inframe deletion, coding sequence variant |
|
rs772264078 |
G>T |
Likely-pathogenic |
Intron variant |
|
rs863225461 |
A>G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs863225462 |
T>C |
Pathogenic |
Missense variant, coding sequence variant |
|
rs863225463 |
A>G |
Pathogenic |
Missense variant, coding sequence variant |
|
rs866727908 |
C>T |
Likely-pathogenic |
Missense variant, genic downstream transcript variant, coding sequence variant, downstream transcript variant |
|
rs878853002 |
C>T |
Pathogenic |
Missense variant, coding sequence variant, intron variant |
|
rs1057518222 |
TGTTGGGGGAG>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs1555596072 |
G>C |
Pathogenic |
Stop gained, coding sequence variant |
|
rs1555596165 |
A>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs1555596483 |
C>T |
Pathogenic |
Splice donor variant |
|
rs1555596757 |
T>C |
Pathogenic |
Splice acceptor variant |
|
rs1567830555 |
C>T |
Likely-pathogenic |
Splice donor variant, intron variant |
|
rs1567834739 |
C>T |
Pathogenic |
Splice donor variant |
|
rs1598299485 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs1598301457 |
->C |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs1598302037 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |