Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565573786
rs1565573786
Entrez Id: 50846;105369759
Gene Symbol: DHH;LOC105369759
DHH;LOC105369759
CUI: C0010417
Disease:
Cryptorchidism
C 0.700 CausalMutation CLINVAR In vitro functional characterization of the novel DHH mutations p.(Asn337Lysfs*24) and p.(Glu212Lys) associated with gonadal dysgenesis. 30298535 2018