rs420038
From SNPedia
Orientation | minus |
Make rs420038(A;A) |
Make rs420038(A;G) |
Make rs420038(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 6 |
Position | 160387116 |
Gene | SLC22A3 |
is a | snp |
is | mentioned by |
dbSNP | rs420038 |
dbSNP (classic) | rs420038 |
ClinGen | rs420038 |
ebi | rs420038 |
HLI | rs420038 |
Exac | rs420038 |
Gnomad | rs420038 |
Varsome | rs420038 |
LitVar | rs420038 |
Map | rs420038 |
PheGenI | rs420038 |
Biobank | rs420038 |
1000 genomes | rs420038 |
hgdp | rs420038 |
ensembl | rs420038 |
geneview | rs420038 |
scholar | rs420038 |
rs420038 | |
pharmgkb | rs420038 |
gwascentral | rs420038 |
openSNP | rs420038 |
23andMe | rs420038 |
SNPshot | rs420038 |
SNPdbe | rs420038 |
MSV3d | rs420038 |
GWAS Ctlg | rs420038 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 30561001] Genetic variants in SLC22A3 contribute to the susceptibility to colorectal cancer.