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rs1423386

From SNPedia

Orientationminus
Stabilizedminus
Make rs1423386(C;C)
Make rs1423386(C;T)
Make rs1423386(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position62689026
is asnp
is mentioned by
dbSNPrs1423386
ebirs1423386
HLIrs1423386
Exacrs1423386
Varsomers1423386
Maprs1423386
PheGenIrs1423386
hapmaprs1423386
1000 genomesrs1423386
hgdprs1423386
ensemblrs1423386
gopubmedrs1423386
geneviewrs1423386
scholarrs1423386
googlers1423386
pharmgkbrs1423386
gwascentralrs1423386
openSNPrs1423386
23andMers1423386
23andMe allrs1423386
SNP Nexus

SNPshotrs1423386
SNPdbers1423386
MSV3drs1423386
GWAS Ctlgrs1423386
GMAF0.2287
Max Magnitude
? (C;C) (C;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 G
P-val 2E-9
Odds Ratio 1.73 [NR]