Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555261576
rs1555261576
Entrez Id: 341640
Gene Symbol: FREM2
FREM2
CUI: C0235833
Disease:
Congenital diaphragmatic hernia
T 0.700 SusceptibilityMutation CLINVAR