Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052954321
rs1052954321
T 0.700 GeneticVariation CLINVAR ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder. 30967659

2019

dbSNP: rs1114167422
rs1114167422
G 0.700 GeneticVariation CLINVAR

dbSNP: rs113993993
rs113993993
G 0.700 CausalMutation CLINVAR

dbSNP: rs120074160
rs120074160
A 0.700 GeneticVariation CLINVAR

dbSNP: rs148636776
rs148636776
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554851718
rs1554851718
FAS
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555366607
rs1555366607
G 0.700 CausalMutation CLINVAR

dbSNP: rs1564691414
rs1564691414
FAS
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1565679039
rs1565679039
A 0.700 CausalMutation CLINVAR

dbSNP: rs1567705064
rs1567705064
G 0.700 CausalMutation CLINVAR

dbSNP: rs41469945
rs41469945
C 0.700 CausalMutation CLINVAR

dbSNP: rs756881285
rs756881285
GC 0.700 CausalMutation CLINVAR

dbSNP: rs770418305
rs770418305
AT 0.700 GeneticVariation CLINVAR

dbSNP: rs77375493
rs77375493
T 0.700 GeneticVariation CLINVAR

dbSNP: rs878853314
rs878853314
GBA
G 0.700 GeneticVariation CLINVAR

dbSNP: rs878853315
rs878853315
GBA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs878853317
rs878853317
GBA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs878853320
rs878853320
GBA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs878853321
rs878853321
GBA
G 0.700 GeneticVariation CLINVAR