FNBP1, formin binding protein 1, 23048

N. diseases: 17; N. variants: 1
Disease: Common Variable Immunodeficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10988542
rs10988542
Entrez Id: 23048
Gene Symbol: FNBP1
FNBP1
CUI: C0009447
Disease:
Common Variable Immunodeficiency 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015