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rs419076

From SNPedia

Orientationplus
Stabilizedplus
Make rs419076(C;C)
Make rs419076(C;T)
Make rs419076(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position169383098
GeneMECOM
is asnp
is mentioned by
dbSNPrs419076
ebirs419076
HLIrs419076
Exacrs419076
Varsomers419076
Maprs419076
PheGenIrs419076
hapmaprs419076
1000 genomesrs419076
hgdprs419076
ensemblrs419076
gopubmedrs419076
geneviewrs419076
scholarrs419076
googlers419076
pharmgkbrs419076
gwascentralrs419076
openSNPrs419076
23andMers419076
23andMe allrs419076
SNP Nexus

SNPshotrs419076
SNPdbers419076
MSV3drs419076
GWAS Ctlgrs419076
GMAF0.4164
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele T
P-val 2E-13
Odds Ratio 0.4090 [NR] mmHg increase
GWAS snp
PMID [PMID 21909110OA-icon.png]
Trait
Title Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Risk Allele T
P-val 8E-13
Odds Ratio 0.3400 [0.25-0.43] mmHg increase