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rs1327235

From SNPedia

Orientationplus
Stabilizedplus
Make rs1327235(A;A)
Make rs1327235(A;G)
Make rs1327235(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position10988382
is asnp
is mentioned by
dbSNPrs1327235
ebirs1327235
HLIrs1327235
Exacrs1327235
Varsomers1327235
Maprs1327235
PheGenIrs1327235
hapmaprs1327235
1000 genomesrs1327235
hgdprs1327235
ensemblrs1327235
gopubmedrs1327235
geneviewrs1327235
scholarrs1327235
googlers1327235
pharmgkbrs1327235
gwascentralrs1327235
openSNPrs1327235
23andMers1327235
23andMe allrs1327235
SNP Nexus

SNPshotrs1327235
SNPdbers1327235
MSV3drs1327235
GWAS Ctlgrs1327235
GMAF0.4679
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele G
P-val 1E-15
Odds Ratio 0.3020 [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 G
P-val 4E-8
Odds Ratio 0.2590 [0.17-0.35] mmHg increase