Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17348614
rs17348614
Entrez Id: 27031;100532724
Gene Symbol: NPHP3;NPHP3-ACAD11
NPHP3;NPHP3-ACAD11
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016