Disease: Forebrain Defects ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909501
rs121909501
Entrez Id: 6997;79442
Gene Symbol: TDGF1;LRRC2
TDGF1;LRRC2
CUI: C1861235
Disease:
Forebrain Defects 		T 0.700 CausalMutation CLINVAR