rs11987193
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11987193(C;C) |
| Make rs11987193(C;T) |
| Make rs11987193(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 8 |
| Position | 29478491 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11987193 |
| dbSNP (classic) | rs11987193 |
| ClinGen | rs11987193 |
| ebi | rs11987193 |
| HLI | rs11987193 |
| Exac | rs11987193 |
| Gnomad | rs11987193 |
| Varsome | rs11987193 |
| LitVar | rs11987193 |
| Map | rs11987193 |
| PheGenI | rs11987193 |
| Biobank | rs11987193 |
| 1000 genomes | rs11987193 |
| hgdp | rs11987193 |
| ensembl | rs11987193 |
| geneview | rs11987193 |
| scholar | rs11987193 |
| rs11987193 | |
| pharmgkb | rs11987193 |
| gwascentral | rs11987193 |
| openSNP | rs11987193 |
| 23andMe | rs11987193 |
| SNPshot | rs11987193 |
| SNPdbe | rs11987193 |
| MSV3d | rs11987193 |
| GWAS Ctlg | rs11987193 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26148620] Genetic variants identified by GWAS was associated with colorectal cancer in the Han Chinese population
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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
