rs6017996
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6017996(A;A) |
| Make rs6017996(A;G) |
| Make rs6017996(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 37358250 |
| Gene | SRC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6017996 |
| dbSNP (classic) | rs6017996 |
| ClinGen | rs6017996 |
| ebi | rs6017996 |
| HLI | rs6017996 |
| Exac | rs6017996 |
| Gnomad | rs6017996 |
| Varsome | rs6017996 |
| LitVar | rs6017996 |
| Map | rs6017996 |
| PheGenI | rs6017996 |
| Biobank | rs6017996 |
| 1000 genomes | rs6017996 |
| hgdp | rs6017996 |
| ensembl | rs6017996 |
| geneview | rs6017996 |
| scholar | rs6017996 |
| rs6017996 | |
| pharmgkb | rs6017996 |
| gwascentral | rs6017996 |
| openSNP | rs6017996 |
| 23andMe | rs6017996 |
| SNPshot | rs6017996 |
| SNPdbe | rs6017996 |
| MSV3d | rs6017996 |
| GWAS Ctlg | rs6017996 |
| GMAF | 0.2144 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23778325
] Impact of genetic polymorphisms on adenoma recurrence and toxicity in a COX2 inhibitor (celecoxib) trial: results from a pilot study
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 20
- 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 Ancestry v2c
- On chip Ancestry v2d
