rs4507975
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4507975(A;A) |
Make rs4507975(A;G) |
Make rs4507975(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 176715296 |
Gene | PAPPA2 |
is a | snp |
is | mentioned by |
dbSNP | rs4507975 |
dbSNP (classic) | rs4507975 |
ClinGen | rs4507975 |
ebi | rs4507975 |
HLI | rs4507975 |
Exac | rs4507975 |
Gnomad | rs4507975 |
Varsome | rs4507975 |
LitVar | rs4507975 |
Map | rs4507975 |
PheGenI | rs4507975 |
Biobank | rs4507975 |
1000 genomes | rs4507975 |
hgdp | rs4507975 |
ensembl | rs4507975 |
geneview | rs4507975 |
scholar | rs4507975 |
rs4507975 | |
pharmgkb | rs4507975 |
gwascentral | rs4507975 |
openSNP | rs4507975 |
23andMe | rs4507975 |
SNPshot | rs4507975 |
SNPdbe | rs4507975 |
MSV3d | rs4507975 |
GWAS Ctlg | rs4507975 |
GMAF | 0.2805 |
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 | |
P-val | 4E-9 |
Odds Ratio | 1.54 [NR] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- 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