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rs4712972

From SNPedia

Orientationplus
Stabilizedplus
Make rs4712972(A;A)
Make rs4712972(A;G)
Make rs4712972(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position25771819
GeneSLC17A4
is asnp
is mentioned by
dbSNPrs4712972
ebirs4712972
HLIrs4712972
Exacrs4712972
Varsomers4712972
Maprs4712972
PheGenIrs4712972
hapmaprs4712972
1000 genomesrs4712972
hgdprs4712972
ensemblrs4712972
gopubmedrs4712972
geneviewrs4712972
scholarrs4712972
googlers4712972
pharmgkbrs4712972
gwascentralrs4712972
openSNPrs4712972
23andMers4712972
23andMe allrs4712972
SNP Nexus

SNPshotrs4712972
SNPdbers4712972
MSV3drs4712972
GWAS Ctlgrs4712972
GMAF0.1974
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21909108OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
Risk Allele A
P-val 8E-8
Odds Ratio 0.0099 [0.01-0.01] unit increase