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rs17477177

From SNPedia

Orientationplus
Stabilizedplus
Make rs17477177(C;C)
Make rs17477177(C;T)
Make rs17477177(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position106771412
is asnp
is mentioned by
dbSNPrs17477177
ebirs17477177
HLIrs17477177
Exacrs17477177
Varsomers17477177
Maprs17477177
PheGenIrs17477177
hapmaprs17477177
1000 genomesrs17477177
hgdprs17477177
ensemblrs17477177
gopubmedrs17477177
geneviewrs17477177
scholarrs17477177
googlers17477177
pharmgkbrs17477177
gwascentralrs17477177
openSNPrs17477177
23andMers17477177
23andMe allrs17477177
SNP Nexus

SNPshotrs17477177
SNPdbers17477177
MSV3drs17477177
GWAS Ctlgrs17477177
GMAF0.1465
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 2E-13
Odds Ratio 0.4180 [0.31-0.53] mmHg decrease