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rs9392653

From SNPedia

Orientationplus
Stabilizedplus
Make rs9392653(C;C)
Make rs9392653(C;T)
Make rs9392653(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position5071258
GeneLYRM4
is asnp
is mentioned by
dbSNPrs9392653
ebirs9392653
HLIrs9392653
Exacrs9392653
Varsomers9392653
Maprs9392653
PheGenIrs9392653
hapmaprs9392653
1000 genomesrs9392653
hgdprs9392653
ensemblrs9392653
gopubmedrs9392653
geneviewrs9392653
scholarrs9392653
googlers9392653
pharmgkbrs9392653
gwascentralrs9392653
openSNPrs9392653
23andMers9392653
23andMe allrs9392653
SNP Nexus

SNPshotrs9392653
SNPdbers9392653
MSV3drs9392653
GWAS Ctlgrs9392653
GMAF0.2406
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 C
P-val 2E-9
Odds Ratio 1.74 [NR]