rs1336708
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1336708(C;C) |
Make rs1336708(C;T) |
Make rs1336708(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 102312653 |
Gene | FGF14, FGF14-IT1, LOC107984615 |
is a | snp |
is | mentioned by |
dbSNP | rs1336708 |
dbSNP (classic) | rs1336708 |
ClinGen | rs1336708 |
ebi | rs1336708 |
HLI | rs1336708 |
Exac | rs1336708 |
Gnomad | rs1336708 |
Varsome | rs1336708 |
LitVar | rs1336708 |
Map | rs1336708 |
PheGenI | rs1336708 |
Biobank | rs1336708 |
1000 genomes | rs1336708 |
hgdp | rs1336708 |
ensembl | rs1336708 |
geneview | rs1336708 |
scholar | rs1336708 |
rs1336708 | |
pharmgkb | rs1336708 |
gwascentral | rs1336708 |
openSNP | rs1336708 |
23andMe | rs1336708 |
SNPshot | rs1336708 |
SNPdbe | rs1336708 |
MSV3d | rs1336708 |
GWAS Ctlg | rs1336708 |
GMAF | 0.2534 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23509962] |
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] |