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rs9804128

From SNPedia

Orientationplus
Stabilizedplus
Make rs9804128(A;A)
Make rs9804128(A;G)
Make rs9804128(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position18098517
is asnp
is mentioned by
dbSNPrs9804128
ebirs9804128
HLIrs9804128
Exacrs9804128
Varsomers9804128
Maprs9804128
PheGenIrs9804128
hapmaprs9804128
1000 genomesrs9804128
hgdprs9804128
ensemblrs9804128
gopubmedrs9804128
geneviewrs9804128
scholarrs9804128
googlers9804128
pharmgkbrs9804128
gwascentralrs9804128
openSNPrs9804128
23andMers9804128
23andMe allrs9804128
SNP Nexus

SNPshotrs9804128
SNPdbers9804128
MSV3drs9804128
GWAS Ctlgrs9804128
GMAF0.3017
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 A
P-val 2E-9
Odds Ratio 1.71 [NR]