Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6769392
rs6769392
Entrez Id: 6997;79442
Gene Symbol: TDGF1;LRRC2
TDGF1;LRRC2
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs121909501
rs121909501
Entrez Id: 6997;79442
Gene Symbol: TDGF1;LRRC2
TDGF1;LRRC2
CUI: C1861235
Disease:
Forebrain Defects 		T 0.700 CausalMutation CLINVAR