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rs971572

From SNPedia

Orientationminus
Stabilizedminus
Make rs971572(G;G)
Make rs971572(G;T)
Make rs971572(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position184099374
is asnp
is mentioned by
dbSNPrs971572
ebirs971572
HLIrs971572
Exacrs971572
Varsomers971572
Maprs971572
PheGenIrs971572
hapmaprs971572
1000 genomesrs971572
hgdprs971572
ensemblrs971572
gopubmedrs971572
geneviewrs971572
scholarrs971572
googlers971572
pharmgkbrs971572
gwascentralrs971572
openSNPrs971572
23andMers971572
23andMe allrs971572
SNP Nexus

SNPshotrs971572
SNPdbers971572
MSV3drs971572
GWAS Ctlgrs971572
GMAF0.3549
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23509962OA-icon.png]
Trait Venous thromboembolism (gene x gene interaction)
Title A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
Risk Allele
P-val 9E-9
Odds Ratio 2.38 [NR]