Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039235
rs886039235
0.800 GeneticVariation UNIPROT Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome. 27426734

2016

dbSNP: rs886039237
rs886039237
0.800 GeneticVariation UNIPROT Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome. 27426734

2016

dbSNP: rs886039235
rs886039235
A 0.800 CausalMutation CLINVAR

dbSNP: rs886039237
rs886039237
T 0.800 CausalMutation CLINVAR

dbSNP: rs886039234
rs886039234
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039236
rs886039236
A 0.700 CausalMutation CLINVAR