rs10504130
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common/normal |
| Make rs10504130(A;A) |
| Make rs10504130(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 51844533 |
| Gene | PCMTD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10504130 |
| dbSNP (classic) | rs10504130 |
| ClinGen | rs10504130 |
| ebi | rs10504130 |
| HLI | rs10504130 |
| Exac | rs10504130 |
| Gnomad | rs10504130 |
| Varsome | rs10504130 |
| LitVar | rs10504130 |
| Map | rs10504130 |
| PheGenI | rs10504130 |
| Biobank | rs10504130 |
| 1000 genomes | rs10504130 |
| hgdp | rs10504130 |
| ensembl | rs10504130 |
| geneview | rs10504130 |
| scholar | rs10504130 |
| rs10504130 | |
| pharmgkb | rs10504130 |
| gwascentral | rs10504130 |
| openSNP | rs10504130 |
| 23andMe | rs10504130 |
| SNPshot | rs10504130 |
| SNPdbe | rs10504130 |
| MSV3d | rs10504130 |
| GWAS Ctlg | rs10504130 |
| GMAF | 0.1299 |
| 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 | G |
| P-val | 4E-9 |
| Odds Ratio | 1.88 [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 Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
