Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10472828
rs10472828
CUI: C0489786
Disease: Height
Height 		C 0.700 GeneticVariation GWASDB A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. 19570815

2009
dbSNP: rs10472828
rs10472828
CUI: C0489786
Disease: Height
Height 		0.700 GeneticVariation GWASDB Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. 19343178

2009