| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs35689779 |
T>C |
Benign, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs61752119 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs61752122 |
TCTCA>- |
Pathogenic |
Coding sequence variant, frameshift variant |
|
rs61752123 |
G>A,C |
Pathogenic |
Coding sequence variant, stop gained, missense variant |
|
rs61752124 |
G>A,T |
Likely-pathogenic, pathogenic |
Coding sequence variant, stop gained, synonymous variant |
|
rs61752127 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
|
rs61752128 |
A>G |
Pathogenic |
Coding sequence variant, missense variant |
|
rs63545361 |
A>- |
Benign, pathogenic |
Coding sequence variant, frameshift variant, missense variant |
|
rs142645936 |
A>C,G |
Uncertain-significance, benign-likely-benign, conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant |
|
rs146354196 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs150734057 |
C>A,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs200065382 |
G>A,T |
Likely-pathogenic, uncertain-significance |
Stop gained, missense variant, coding sequence variant |
|
rs267608188 |
AAGTA>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs367649632 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, coding sequence variant |
|
rs375401977 |
A>C |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
|
rs376101275 |
T>A,C,G |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
|
rs724160029 |
->T |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs764771123 |
TGCCACC>- |
Pathogenic-likely-pathogenic, likely-pathogenic, pathogenic |
Frameshift variant, coding sequence variant |
|
rs764785488 |
A>G |
Conflicting-interpretations-of-pathogenicity |
Synonymous variant, coding sequence variant |
|
rs886039481 |
C>T |
Pathogenic |
Coding sequence variant, missense variant |
|
rs1235008965 |
->T |
Pathogenic-likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1438831421 |
->T |
Pathogenic-likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1554584474 |
CT>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1554584487 |
G>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1554584505 |
GT>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1586069639 |
A>T |
Pathogenic |
Coding sequence variant, stop gained |
|
rs1586070043 |
G>A |
Pathogenic |
Coding sequence variant, stop gained |
|
rs1586070089 |
T>- |
Pathogenic |
Coding sequence variant, frameshift variant |