rs12541254
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12541254(A;A) |
Make rs12541254(A;G) |
Make rs12541254(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 13121891 |
Gene | DLC1 |
is a | snp |
is | mentioned by |
dbSNP | rs12541254 |
dbSNP (classic) | rs12541254 |
ClinGen | rs12541254 |
ebi | rs12541254 |
HLI | rs12541254 |
Exac | rs12541254 |
Gnomad | rs12541254 |
Varsome | rs12541254 |
LitVar | rs12541254 |
Map | rs12541254 |
PheGenI | rs12541254 |
Biobank | rs12541254 |
1000 genomes | rs12541254 |
hgdp | rs12541254 |
ensembl | rs12541254 |
geneview | rs12541254 |
scholar | rs12541254 |
rs12541254 | |
pharmgkb | rs12541254 |
gwascentral | rs12541254 |
openSNP | rs12541254 |
23andMe | rs12541254 |
SNPshot | rs12541254 |
SNPdbe | rs12541254 |
MSV3d | rs12541254 |
GWAS Ctlg | rs12541254 |
GMAF | 0.2778 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 3E-9 |
Odds Ratio | 1.65 [NR] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 8
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d