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rs7591163

From SNPedia

Orientationplus
Stabilizedplus
Make rs7591163(C;C)
Make rs7591163(C;T)
Make rs7591163(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position227850659
is asnp
is mentioned by
dbSNPrs7591163
dbSNP (classic)rs7591163
ClinGenrs7591163
ebirs7591163
HLIrs7591163
Exacrs7591163
Gnomadrs7591163
Varsomers7591163
LitVarrs7591163
Maprs7591163
PheGenIrs7591163
Biobankrs7591163
1000 genomesrs7591163
hgdprs7591163
ensemblrs7591163
geneviewrs7591163
scholarrs7591163
googlers7591163
pharmgkbrs7591163
gwascentralrs7591163
openSNPrs7591163
23andMers7591163
SNPshotrs7591163
SNPdbers7591163
MSV3drs7591163
GWAS Ctlgrs7591163
GMAF0.3554
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Blood pressure
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 2.9999999999999999E-7
Odds Ratio NR NR