SFXN2, sideroflexin 2, 118980

N. diseases: 5; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2902548
rs2902548
Entrez Id: 118980
Gene Symbol: SFXN2
SFXN2
CUI: C0524587
Disease:
Mean Corpuscular Volume (result)
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018