rs11195128
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11195128(C;C) |
| Make rs11195128(C;T) |
| Make rs11195128(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 110426390 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11195128 |
| dbSNP (classic) | rs11195128 |
| ClinGen | rs11195128 |
| ebi | rs11195128 |
| HLI | rs11195128 |
| Exac | rs11195128 |
| Gnomad | rs11195128 |
| Varsome | rs11195128 |
| LitVar | rs11195128 |
| Map | rs11195128 |
| PheGenI | rs11195128 |
| Biobank | rs11195128 |
| 1000 genomes | rs11195128 |
| hgdp | rs11195128 |
| ensembl | rs11195128 |
| geneview | rs11195128 |
| scholar | rs11195128 |
| rs11195128 | |
| pharmgkb | rs11195128 |
| gwascentral | rs11195128 |
| openSNP | rs11195128 |
| 23andMe | rs11195128 |
| SNPshot | rs11195128 |
| SNPdbe | rs11195128 |
| MSV3d | rs11195128 |
| GWAS Ctlg | rs11195128 |
| GMAF | 0.2332 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23850713] Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- 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
