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rs899997

From SNPedia

Orientationminus
Stabilizedminus
Make rs899997(A;A)
Make rs899997(A;C)
Make rs899997(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position78727236
is asnp
is mentioned by
dbSNPrs899997
ebirs899997
HLIrs899997
Exacrs899997
Varsomers899997
Maprs899997
PheGenIrs899997
hapmaprs899997
1000 genomesrs899997
hgdprs899997
ensemblrs899997
gopubmedrs899997
geneviewrs899997
scholarrs899997
googlers899997
pharmgkbrs899997
gwascentralrs899997
openSNPrs899997
23andMers899997
23andMe allrs899997
SNP Nexus

SNPshotrs899997
SNPdbers899997
MSV3drs899997
GWAS Ctlgrs899997
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease or large artery stroke
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele
P-val 2E-8
Odds Ratio NR NR