Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565308384
rs1565308384
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
CA 0.700 CausalMutation CLINVAR