rs4979078
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4979078(C;C) |
Make rs4979078(C;T) |
Make rs4979078(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 112060841 |
Gene | SUSD1 |
is a | snp |
is | mentioned by |
dbSNP | rs4979078 |
dbSNP (classic) | rs4979078 |
ClinGen | rs4979078 |
ebi | rs4979078 |
HLI | rs4979078 |
Exac | rs4979078 |
Gnomad | rs4979078 |
Varsome | rs4979078 |
LitVar | rs4979078 |
Map | rs4979078 |
PheGenI | rs4979078 |
Biobank | rs4979078 |
1000 genomes | rs4979078 |
hgdp | rs4979078 |
ensembl | rs4979078 |
geneview | rs4979078 |
scholar | rs4979078 |
rs4979078 | |
pharmgkb | rs4979078 |
gwascentral | rs4979078 |
openSNP | rs4979078 |
23andMe | rs4979078 |
SNPshot | rs4979078 |
SNPdbe | rs4979078 |
MSV3d | rs4979078 |
GWAS Ctlg | rs4979078 |
GMAF | 0.2893 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23650146] |
Trait | Venous thromboembolism |
Title | A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. |
Risk Allele | C |
P-val | 3E-6 |
Odds Ratio | 1.21 [1.11-1.30] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- 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