Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11191548
rs11191548
CNNM2
0.020 GeneticVariation BEFREE Methods We investigated the SNP rs11191548 in a case-control study of 1,102 subjects with essential hypertension (EH) and 1,109 normotensive controls. 23467202

2013
dbSNP: rs11191548
rs11191548
CNNM2
0.020 GeneticVariation BEFREE Whether the nominally significant associations for rs12946454 and rs11191548 are true signals and could be of possible clinical relevance for deciding treatment of polygenic essential hypertension should be further tested. 22525200

2012