Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs762292772
rs762292772
TG 0.700 CausalMutation CLINVAR Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions. 25356970

2015

dbSNP: rs1085308043
rs1085308043
G 0.700 CausalMutation CLINVAR

dbSNP: rs121909219
rs121909219
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909224
rs121909224
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909231
rs121909231
T 0.700 CausalMutation CLINVAR

dbSNP: rs1276388879
rs1276388879
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1372713010
rs1372713010
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1418634444
rs1418634444
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1452048149
rs1452048149
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1476293577
rs1476293577
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1484207450
rs1484207450
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1557863430
rs1557863430
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557863440
rs1557863440
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557863546
rs1557863546
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1557867853
rs1557867853
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1557870645
rs1557870645
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1557874046
rs1557874046
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1557901347
rs1557901347
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557902023
rs1557902023
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557909572
rs1557909572
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557909821
rs1557909821
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1557910728
rs1557910728
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557911386
rs1557911386
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1557916296
rs1557916296
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1557935477
rs1557935477
T 0.700 GeneticVariation CLINVAR