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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
ebirs7591163
HLIrs7591163
Exacrs7591163
Varsomers7591163
Maprs7591163
PheGenIrs7591163
hapmaprs7591163
1000 genomesrs7591163
hgdprs7591163
ensemblrs7591163
gopubmedrs7591163
geneviewrs7591163
scholarrs7591163
googlers7591163
pharmgkbrs7591163
gwascentralrs7591163
openSNPrs7591163
23andMers7591163
23andMe allrs7591163
SNP Nexus

SNPshotrs7591163
SNPdbers7591163
MSV3drs7591163
GWAS Ctlgrs7591163
GMAF0.3554
Max Magnitude
? (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


GET Evidence
rs7591163
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.726562
summary