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rs7152623

From SNPedia

Orientationplus
Stabilizedplus
Make rs7152623(A;A)
Make rs7152623(A;G)
Make rs7152623(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position98121984
is asnp
is mentioned by
dbSNPrs7152623
ebirs7152623
HLIrs7152623
Exacrs7152623
Varsomers7152623
Maprs7152623
PheGenIrs7152623
hapmaprs7152623
1000 genomesrs7152623
hgdprs7152623
ensemblrs7152623
gopubmedrs7152623
geneviewrs7152623
scholarrs7152623
googlers7152623
pharmgkbrs7152623
gwascentralrs7152623
openSNPrs7152623
23andMers7152623
23andMe allrs7152623
SNP Nexus

SNPshotrs7152623
SNPdbers7152623
MSV3drs7152623
GWAS Ctlgrs7152623
GMAF0.2911
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22068335OA-icon.png]
Trait
Title Common Genetic Variation in the 3'-BCL11B Gene Desert Is Associated With Carotid-Femoral Pulse Wave Velocity and Excess Cardiovascular Disease Risk: The AortaGen Consortium.
Risk Allele
P-val 3E-15
Odds Ratio 0.0760 None