TMEM258, transmembrane protein 258, 746

N. diseases: 63; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs174533
rs174533
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0518015
Disease:
Hemoglobin measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016