SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs111266804 |
G>A,C |
Likely-pathogenic |
Splice donor variant |
rs113803159 |
C>G |
Conflicting-interpretations-of-pathogenicity, likely-benign |
Synonymous variant, coding sequence variant |
rs117350233 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
rs121918113 |
C>T |
Pathogenic |
Coding sequence variant, stop gained |
rs121918114 |
C>A |
Pathogenic |
Coding sequence variant, stop gained |
rs121918115 |
C>G,T |
Uncertain-significance, pathogenic |
Coding sequence variant, missense variant |
rs398124554 |
C>- |
Uncertain-significance, pathogenic |
Frameshift variant, coding sequence variant |
rs398124555 |
->T |
Uncertain-significance, pathogenic |
Frameshift variant, coding sequence variant |
rs551660089 |
G>A |
Likely-pathogenic, pathogenic |
Splice donor variant |
rs748241465 |
C>- |
Pathogenic |
Frameshift variant, coding sequence variant |
rs751365374 |
C>-,CC,CCC |
Pathogenic-likely-pathogenic, likely-pathogenic, pathogenic |
Frameshift variant, coding sequence variant |
rs755227074 |
G>A |
Likely-pathogenic |
Splice donor variant |
rs895911431 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
rs897301304 |
C>T |
Pathogenic, likely-pathogenic |
Stop gained, coding sequence variant |
rs972494690 |
G>A,T |
Pathogenic |
Coding sequence variant, stop gained, missense variant |
rs1409892710 |
T>G |
Pathogenic |
Stop gained, coding sequence variant |
rs1421005631 |
CT>- |
Pathogenic |
Frameshift variant, coding sequence variant |
rs1555515558 |
TGTGGCTGCCAT>ACGGCATA |
Pathogenic |
Frameshift variant, coding sequence variant |
rs1555516994 |
C>T |
Likely-pathogenic |
Stop gained, coding sequence variant |
rs1567479853 |
A>T |
Likely-pathogenic |
Splice acceptor variant |
rs1596682330 |
GGT>TGG |
Likely-pathogenic |
Splice donor variant, coding sequence variant |