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rs4714955

From SNPedia

Orientationplus
Stabilizedplus
Make rs4714955(C;C)
Make rs4714955(C;T)
Make rs4714955(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position12903203
GenePHACTR1
is asnp
is mentioned by
dbSNPrs4714955
ebirs4714955
HLIrs4714955
Exacrs4714955
Varsomers4714955
Maprs4714955
PheGenIrs4714955
hapmaprs4714955
1000 genomesrs4714955
hgdprs4714955
ensemblrs4714955
gopubmedrs4714955
geneviewrs4714955
scholarrs4714955
googlers4714955
pharmgkbrs4714955
gwascentralrs4714955
openSNPrs4714955
23andMers4714955
23andMe allrs4714955
SNP Nexus

SNPshotrs4714955
SNPdbers4714955
MSV3drs4714955
GWAS Ctlgrs4714955
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease or ischemic stroke
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele
P-val 4E-11
Odds Ratio NR NR