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rs1910358

From SNPedia

Orientationplus
Stabilizedplus
Make rs1910358(C;C)
Make rs1910358(C;T)
Make rs1910358(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position23907464
is asnp
is mentioned by
dbSNPrs1910358
ebirs1910358
HLIrs1910358
Exacrs1910358
Varsomers1910358
Maprs1910358
PheGenIrs1910358
hapmaprs1910358
1000 genomesrs1910358
hgdprs1910358
ensemblrs1910358
gopubmedrs1910358
geneviewrs1910358
scholarrs1910358
googlers1910358
pharmgkbrs1910358
gwascentralrs1910358
openSNPrs1910358
23andMers1910358
23andMe allrs1910358
SNP Nexus

SNPshotrs1910358
SNPdbers1910358
MSV3drs1910358
GWAS Ctlgrs1910358
GMAF0.3095
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 7E-9
Odds Ratio 2.03 [NR]