Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13097314
rs13097314
Entrez Id: 131177
Gene Symbol: FAM3D
FAM3D
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs3749290
rs3749290
Entrez Id: 131177;105377109
Gene Symbol: FAM3D;LOC105377109
FAM3D;LOC105377109
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs6807381
rs6807381
Entrez Id: 131177;105377109
Gene Symbol: FAM3D;LOC105377109
FAM3D;LOC105377109
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs11130665
rs11130665
Entrez Id: 131177
Gene Symbol: FAM3D
FAM3D
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017