| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
| rs28933687 |
G>A,T |
Pathogenic |
Coding sequence variant, missense variant |
| rs104894925 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
| rs104894926 |
C>G |
Pathogenic |
Coding sequence variant, stop gained |
| rs104894927 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
| rs137852284 |
TCC>- |
Pathogenic |
Coding sequence variant, inframe deletion |
| rs398124239 |
C>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs782103396 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant |
| rs782344765 |
G>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
| rs797044507 |
C>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs797044561 |
T>C |
Likely-pathogenic, pathogenic |
Initiator codon variant, missense variant |
| rs878853381 |
T>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
| rs886044897 |
AT>- |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs1064797368 |
G>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
| rs1556313414 |
TCT>- |
Likely-pathogenic |
Inframe deletion, coding sequence variant |
| rs1556313474 |
T>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
| rs1556313530 |
->CA |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs1556313552 |
G>A |
Likely-pathogenic |
Synonymous variant, coding sequence variant |
| rs1556313557 |
A>C |
Pathogenic |
Intron variant |
| rs1556318579 |
->TACC |
Pathogenic |
Frameshift variant, coding sequence variant |
| rs1556318627 |
C>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs1556318633 |
C>G,T |
Pathogenic, likely-pathogenic |
Missense variant, coding sequence variant |
| rs1556318642 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
| rs1569531639 |
AGGGC>- |
Pathogenic |
Coding sequence variant, frameshift variant |
| rs1602342597 |
CGGA>- |
Pathogenic |
Coding sequence variant, frameshift variant |
| rs1602342663 |
G>T |
Pathogenic |
Splice donor variant |
| rs1602347637 |
T>- |
Pathogenic |
Coding sequence variant, frameshift variant |
| rs1602347741 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
| rs1602347786 |
T>- |
Pathogenic |
Coding sequence variant, frameshift variant |
| rs1602347792 |
T>A |
Likely-pathogenic |
Coding sequence variant, stop gained |
| rs1602347851 |
TT>- |
Pathogenic |
Coding sequence variant, frameshift variant |
| rs1602347992 |
T>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
| rs1602349705 |
G>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
| rs1602355025 |
G>- |
Pathogenic |
Coding sequence variant, frameshift variant |