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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
dbSNP (classic)rs971572
ClinGenrs971572
ebirs971572
HLIrs971572
Exacrs971572
Gnomadrs971572
Varsomers971572
LitVarrs971572
Maprs971572
PheGenIrs971572
Biobankrs971572
1000 genomesrs971572
hgdprs971572
ensemblrs971572
geneviewrs971572
scholarrs971572
googlers971572
pharmgkbrs971572
gwascentralrs971572
openSNPrs971572
23andMers971572
SNPshotrs971572
SNPdbers971572
MSV3drs971572
GWAS Ctlgrs971572
GMAF0.3549
Max Magnitude0
? (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]