| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
| rs372174278 |
G>C,T |
Pathogenic |
Missense variant, coding sequence variant |
| rs558425417 |
T>A,C |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs730880255 |
A>T |
Pathogenic |
Coding sequence variant, missense variant |
| rs748022451 |
G>C,T |
Likely-pathogenic |
Intron variant |
| rs765129583 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs770871640 |
T>C |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs774708853 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs869320746 |
->C |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs886037734 |
G>A |
Pathogenic |
Missense variant, coding sequence variant |
| rs886037735 |
G>C |
Pathogenic |
Missense variant, intron variant, coding sequence variant |
| rs886037736 |
AA>GTG |
Pathogenic |
Frameshift variant, intron variant, coding sequence variant |
| rs886041488 |
T>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs1019249439 |
T>A,C,G |
Pathogenic |
Intron variant, missense variant, initiator codon variant |
| rs1274363168 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant |
| rs1555726849 |
G>T |
Pathogenic |
Coding sequence variant, stop gained |
| rs1599560256 |
G>T |
Pathogenic |
Coding sequence variant, stop gained |
|