| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
| rs655423 |
G>A,C |
Pathogenic |
Splice donor variant |
| rs368970014 |
C>G,T |
Pathogenic |
Synonymous variant, stop gained, coding sequence variant |
| rs397514508 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
| rs397514509 |
C>A,G,T |
Pathogenic |
Missense variant, stop gained, coding sequence variant |
| rs397514510 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
| rs397514511 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
| rs397514512 |
T>A |
Pathogenic |
Missense variant, coding sequence variant |
| rs746647683 |
AG>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs797044468 |
A>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs797044469 |
AGACC>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs797044470 |
GAGGAGCTGCTGGCCCGGGCGGGCCGCG>- |
Pathogenic |
Frameshift variant, coding sequence variant, 5 prime UTR variant |
| rs878853119 |
GGGCCCGGGGGGCGCC>- |
Pathogenic |
Frameshift variant, coding sequence variant, 5 prime UTR variant |
| rs878853120 |
G>C |
Pathogenic |
Missense variant, coding sequence variant |
| rs878853121 |
ACCTC>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs878853122 |
->G |
Pathogenic |
Frameshift variant, coding sequence variant, 5 prime UTR variant |
| rs878853123 |
C>T |
Pathogenic |
Missense variant, coding sequence variant |
| rs1135401750 |
->T |
Pathogenic |
Coding sequence variant, frameshift variant |
| rs1135401751 |
G>- |
Pathogenic |
Coding sequence variant, frameshift variant |