Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs772395858
rs772395858
C 0.700 GeneticVariation CLINVAR The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency. 11181649

2001

dbSNP: rs776641008
rs776641008
A 0.700 CausalMutation CLINVAR The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency. 11181649

2001

dbSNP: rs1311374961
rs1311374961
C 0.700 CausalMutation CLINVAR

dbSNP: rs150862707
rs150862707
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553850609
rs1553850609
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553856095
rs1553856095
T 0.700 CausalMutation CLINVAR

dbSNP: rs1560224024
rs1560224024
G 0.700 CausalMutation CLINVAR

dbSNP: rs1560256569
rs1560256569
GCTATGCTAT 0.700 CausalMutation CLINVAR

dbSNP: rs185741664
rs185741664
A 0.700 CausalMutation CLINVAR

dbSNP: rs199914879
rs199914879
T 0.700 CausalMutation CLINVAR

dbSNP: rs398124350
rs398124350
G 0.700 CausalMutation CLINVAR

dbSNP: rs750484977
rs750484977
C 0.700 CausalMutation CLINVAR

dbSNP: rs754460336
rs754460336
A 0.700 GeneticVariation CLINVAR

dbSNP: rs762463914
rs762463914
C 0.700 GeneticVariation CLINVAR

dbSNP: rs796051985
rs796051985
C 0.700 CausalMutation CLINVAR

dbSNP: rs886058209
rs886058209
T 0.700 CausalMutation CLINVAR

dbSNP: rs920162850
rs920162850
A 0.700 CausalMutation CLINVAR