| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
| rs104893969 |
C>T |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
| rs104893970 |
G>A |
Pathogenic |
Intron variant, coding sequence variant, missense variant, 5 prime UTR variant |
| rs140243105 |
C>G,T |
Conflicting-interpretations-of-pathogenicity, uncertain-significance, likely-benign |
Missense variant, non coding transcript variant, coding sequence variant |
| rs141982812 |
C>T |
Pathogenic |
Splice donor variant |
| rs146075796 |
C>A,T |
Pathogenic |
Splice donor variant |
| rs148579886 |
G>A |
Likely-benign, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, non coding transcript variant, missense variant |
| rs372246702 |
C>A,T |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
| rs377167949 |
G>A |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
| rs397518418 |
A>- |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant |
| rs397518419 |
CT>- |
Likely-pathogenic |
Non coding transcript variant, frameshift variant, 3 prime UTR variant, coding sequence variant |
| rs752653792 |
C>T |
Likely-pathogenic |
Intron variant |
| rs886042028 |
GATGGCCTTGTGGATGCCCTC>- |
Pathogenic |
Inframe deletion, coding sequence variant, non coding transcript variant |
| rs1562085332 |
T>A |
Likely-pathogenic |
Coding sequence variant, stop gained, intron variant |
|