TNFSF18, TNF superfamily member 18, 8995

N. diseases: 15; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9286880
rs9286880
Entrez Id: 8995
Gene Symbol: TNFSF18
TNFSF18
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013