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rs6771316

From SNPedia

Orientationplus
Stabilizedplus
Make rs6771316(A;A)
Make rs6771316(A;G)
Make rs6771316(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position72091381
GeneLINC00877
is asnp
is mentioned by
dbSNPrs6771316
ebirs6771316
HLIrs6771316
Exacrs6771316
Varsomers6771316
Maprs6771316
PheGenIrs6771316
hapmaprs6771316
1000 genomesrs6771316
hgdprs6771316
ensemblrs6771316
gopubmedrs6771316
geneviewrs6771316
scholarrs6771316
googlers6771316
pharmgkbrs6771316
gwascentralrs6771316
openSNPrs6771316
23andMers6771316
23andMe allrs6771316
SNP Nexus

SNPshotrs6771316
SNPdbers6771316
MSV3drs6771316
GWAS Ctlgrs6771316
GMAF0.112
Max Magnitude
? (A;A) (A;G) (G;G) 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 5E-9
Odds Ratio 2.13 [NR]