rs2504916
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2504916(A;A) |
Make rs2504916(A;T) |
Make rs2504916(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 160402996 |
Gene | SLC22A3 |
is a | snp |
is | mentioned by |
dbSNP | rs2504916 |
dbSNP (classic) | rs2504916 |
ClinGen | rs2504916 |
ebi | rs2504916 |
HLI | rs2504916 |
Exac | rs2504916 |
Gnomad | rs2504916 |
Varsome | rs2504916 |
LitVar | rs2504916 |
Map | rs2504916 |
PheGenI | rs2504916 |
Biobank | rs2504916 |
1000 genomes | rs2504916 |
hgdp | rs2504916 |
ensembl | rs2504916 |
geneview | rs2504916 |
scholar | rs2504916 |
rs2504916 | |
pharmgkb | rs2504916 |
gwascentral | rs2504916 |
openSNP | rs2504916 |
23andMe | rs2504916 |
SNPshot | rs2504916 |
SNPdbe | rs2504916 |
MSV3d | rs2504916 |
GWAS Ctlg | rs2504916 |
GMAF | 0.1515 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22095909] |
Trait | |
Title | Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy. |
Risk Allele | T |
P-val | 0.000002 |
Odds Ratio | 0.3060 None |