rs6018257
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6018257(C;C) |
Make rs6018257(C;T) |
Make rs6018257(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 37394136 |
Gene | SRC |
is a | snp |
is | mentioned by |
dbSNP | rs6018257 |
dbSNP (classic) | rs6018257 |
ClinGen | rs6018257 |
ebi | rs6018257 |
HLI | rs6018257 |
Exac | rs6018257 |
Gnomad | rs6018257 |
Varsome | rs6018257 |
LitVar | rs6018257 |
Map | rs6018257 |
PheGenI | rs6018257 |
Biobank | rs6018257 |
1000 genomes | rs6018257 |
hgdp | rs6018257 |
ensembl | rs6018257 |
geneview | rs6018257 |
scholar | rs6018257 |
rs6018257 | |
pharmgkb | rs6018257 |
gwascentral | rs6018257 |
openSNP | rs6018257 |
23andMe | rs6018257 |
SNPshot | rs6018257 |
SNPdbe | rs6018257 |
MSV3d | rs6018257 |
GWAS Ctlg | rs6018257 |
GMAF | 0.2264 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23778325] Impact of genetic polymorphisms on adenoma recurrence and toxicity in a COX2 inhibitor (celecoxib) trial: results from a pilot study