Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1327062642
rs1327062642
TG 0.700 CausalMutation CLINVAR Antioxidant effect of aqueous extract of four plants with therapeutic potential on gynecological diseases; Semen persicae, Leonurus cardiaca, Hedyotis diffusa, and Curcuma zedoaria. 29178942

2017

dbSNP: rs1554333853
rs1554333853
G 0.700 GeneticVariation CLINVAR Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders. 28807008

2017

dbSNP: rs151344517
rs151344517
T 0.700 CausalMutation CLINVAR Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. 20725928

2010

dbSNP: rs121908557
rs121908557
T 0.700 CausalMutation CLINVAR [The construction and preliminary investigation of the cell model of a novel mutation R675Q in the SCN4A gene identified in a Chinese family with normokalemic periodic paralysis]. 19065518

2008

dbSNP: rs121908557
rs121908557
T 0.700 CausalMutation CLINVAR New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. 15596759

2004

dbSNP: rs1009298200
rs1009298200
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518843
rs1057518843
T 0.700 GeneticVariation CLINVAR

dbSNP: rs11555217
rs11555217
T 0.700 CausalMutation CLINVAR

dbSNP: rs119473033
rs119473033
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913482
rs121913482
T 0.700 CausalMutation CLINVAR

dbSNP: rs1344172059
rs1344172059
T 0.700 GeneticVariation CLINVAR

dbSNP: rs137854889
rs137854889
GT 0.700 CausalMutation CLINVAR

dbSNP: rs141322087
rs141322087
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1441937959
rs1441937959
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553655558
rs1553655558
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554199368
rs1554199368
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555452127
rs1555452127
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555575860
rs1555575860
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555727493
rs1555727493
TGGCGGCGGCGGCG 0.700 CausalMutation CLINVAR

dbSNP: rs1555954284
rs1555954284
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1559470315
rs1559470315
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1559931177
rs1559931177
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563183492
rs1563183492
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1564062144
rs1564062144
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569355102
rs1569355102
T 0.700 CausalMutation CLINVAR