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rs13082711

From SNPedia

Orientationplus
Stabilizedplus
Make rs13082711(C;C)
Make rs13082711(C;T)
Make rs13082711(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position27496418
is asnp
is mentioned by
dbSNPrs13082711
ebirs13082711
HLIrs13082711
Exacrs13082711
Varsomers13082711
Maprs13082711
PheGenIrs13082711
hapmaprs13082711
1000 genomesrs13082711
hgdprs13082711
ensemblrs13082711
gopubmedrs13082711
geneviewrs13082711
scholarrs13082711
googlers13082711
pharmgkbrs13082711
gwascentralrs13082711
openSNPrs13082711
23andMers13082711
23andMe allrs13082711
SNP Nexus

SNPshotrs13082711
SNPdbers13082711
MSV3drs13082711
GWAS Ctlgrs13082711
GMAF0.1194
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 4E-9
Odds Ratio 0.2380 [NR] mmHg decrease
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 5E-9
Odds Ratio 0.3360 [0.22-0.45] mmHg decrease


[PMID 27508834] [OP.7C.02] BLOOD PRESSURE-ASSOCIATED POLYMORPHISMS IN SLC4A7 (SODIUM/BICARBONATE CO-TRANSPORTER NBCN1) ARE LINKED WITH GENE EXPRESSION AND INTRACELLULAR PH REGULATION.