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rs5943057

From SNPedia

Orientationplus
Stabilizedplus
Make rs5943057(G;G)
Make rs5943057(G;T)
Make rs5943057(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position110695977
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs5943057
ebirs5943057
HLIrs5943057
Exacrs5943057
Varsomers5943057
Maprs5943057
PheGenIrs5943057
hapmaprs5943057
1000 genomesrs5943057
hgdprs5943057
ensemblrs5943057
gopubmedrs5943057
geneviewrs5943057
scholarrs5943057
googlers5943057
pharmgkbrs5943057
gwascentralrs5943057
openSNPrs5943057
23andMers5943057
23andMe allrs5943057
SNP Nexus

SNPshotrs5943057
SNPdbers5943057
MSV3drs5943057
GWAS Ctlgrs5943057
GMAF0.3718
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 21378988]
Trait
Title A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Risk Allele
P-val 9E-7
Odds Ratio None None