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rs1336708

From SNPedia

Orientationminus
Stabilizedminus
Make rs1336708(C;C)
Make rs1336708(C;T)
Make rs1336708(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position102312653
GeneFGF14, FGF14-IT1, LOC107984615
is asnp
is mentioned by
dbSNPrs1336708
dbSNP (classic)rs1336708
ClinGenrs1336708
ebirs1336708
HLIrs1336708
Exacrs1336708
Gnomadrs1336708
Varsomers1336708
LitVarrs1336708
Maprs1336708
PheGenIrs1336708
Biobankrs1336708
1000 genomesrs1336708
hgdprs1336708
ensemblrs1336708
geneviewrs1336708
scholarrs1336708
googlers1336708
pharmgkbrs1336708
gwascentralrs1336708
openSNPrs1336708
23andMers1336708
SNPshotrs1336708
SNPdbers1336708
MSV3drs1336708
GWAS Ctlgrs1336708
GMAF0.2534
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 5E-9
Odds Ratio 1.72 [NR]