Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs662735
rs662735
Entrez Id: 341019;105376611
Gene Symbol: DCDC1;LOC105376611
DCDC1;LOC105376611
CUI: C0018935
Disease:
Hematocrit procedure
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016