Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518697
rs1057518697
A 0.800 GeneticVariation CLINVAR Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C. 23356856

2013

dbSNP: rs1057518697
rs1057518697
0.800 GeneticVariation UNIPROT

dbSNP: rs199422234
rs199422234
A 0.800 CausalMutation CLINVAR

dbSNP: rs199422234
rs199422234
0.800 GeneticVariation UNIPROT

dbSNP: rs199422235
rs199422235
0.800 GeneticVariation UNIPROT

dbSNP: rs199422235
rs199422235
G 0.800 CausalMutation CLINVAR

dbSNP: rs199422237
rs199422237
0.800 GeneticVariation UNIPROT

dbSNP: rs199422237
rs199422237
C 0.800 CausalMutation CLINVAR

dbSNP: rs1057517955
rs1057517955
0.700 GeneticVariation UNIPROT

dbSNP: rs1057519393
rs1057519393
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1060499661
rs1060499661
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131692227
rs1131692227
T 0.700 CausalMutation CLINVAR

dbSNP: rs1135401800
rs1135401800
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556842184
rs1556842184
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556852362
rs1556852362
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569258293
rs1569258293
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569278313
rs1569278313
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569278313
rs1569278313
T 0.700 CausalMutation CLINVAR

dbSNP: rs1569279367
rs1569279367
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569285361
rs1569285361
A 0.700 GeneticVariation CLINVAR

dbSNP: rs199422236
rs199422236
A 0.700 CausalMutation CLINVAR

dbSNP: rs199422238
rs199422238
A 0.700 CausalMutation CLINVAR

dbSNP: rs199422239
rs199422239
T 0.700 CausalMutation CLINVAR

dbSNP: rs281860639
rs281860639
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906729
rs387906729
T 0.700 CausalMutation CLINVAR