CFHR4, complement factor H related 4, 10877

N. diseases: 11; N. variants: 15
Disease: Hemopexin measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10494745
rs10494745
Entrez Id: 10877;105371675
Gene Symbol: CFHR4;LOC105371675
CFHR4;LOC105371675
CUI: C0523688
Disease:
Hemopexin measurement 		A 0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269 2017