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rs7129220

From SNPedia

Orientationplus
Stabilizedplus
Make rs7129220(A;A)
Make rs7129220(A;G)
Make rs7129220(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position10328991
GeneCAND1.11
is asnp
is mentioned by
dbSNPrs7129220
ebirs7129220
HLIrs7129220
Exacrs7129220
Varsomers7129220
Maprs7129220
PheGenIrs7129220
hapmaprs7129220
1000 genomesrs7129220
hgdprs7129220
ensemblrs7129220
gopubmedrs7129220
geneviewrs7129220
scholarrs7129220
googlers7129220
pharmgkbrs7129220
gwascentralrs7129220
openSNPrs7129220
23andMers7129220
23andMe allrs7129220
SNP Nexus

SNPshotrs7129220
SNPdbers7129220
MSV3drs7129220
GWAS Ctlgrs7129220
GMAF0.073
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 6E-8
Odds Ratio 0.2990 [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 G
P-val 4E-7
Odds Ratio 0.3800 [0.23-0.53] mmHg decrease


[PMID 19039035OA-icon.png] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.