Gene: CCDC92 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11057401
rs11057401
CCDC92
0.010 GeneticVariation BEFREE The genotypic and allelic frequencies of the rs11057401 SNP were significantly different between the patients with CHD and controls. 29439709

2018