| 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 |