Have questions? Visit https://www.reddit.com/r/SNPedia

rs2710201

From SNPedia

Orientationminus
Stabilizedminus
Make rs2710201(C;C)
Make rs2710201(C;T)
Make rs2710201(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position153227808
GeneLOC102723686
is asnp
is mentioned by
dbSNPrs2710201
dbSNP (classic)rs2710201
ClinGenrs2710201
ebirs2710201
HLIrs2710201
Exacrs2710201
Gnomadrs2710201
Varsomers2710201
LitVarrs2710201
Maprs2710201
PheGenIrs2710201
Biobankrs2710201
1000 genomesrs2710201
hgdprs2710201
ensemblrs2710201
geneviewrs2710201
scholarrs2710201
googlers2710201
pharmgkbrs2710201
gwascentralrs2710201
openSNPrs2710201
23andMers2710201
SNPshotrs2710201
SNPdbers2710201
MSV3drs2710201
GWAS Ctlgrs2710201
GMAF0.2075
Max Magnitude0
? (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
P-val 3E-9
Odds Ratio 2.50 [NR]