rs12527818
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12527818(C;C) |
Make rs12527818(C;T) |
Make rs12527818(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 93201401 |
is a | snp |
is | mentioned by |
dbSNP | rs12527818 |
dbSNP (classic) | rs12527818 |
ClinGen | rs12527818 |
ebi | rs12527818 |
HLI | rs12527818 |
Exac | rs12527818 |
Gnomad | rs12527818 |
Varsome | rs12527818 |
LitVar | rs12527818 |
Map | rs12527818 |
PheGenI | rs12527818 |
Biobank | rs12527818 |
1000 genomes | rs12527818 |
hgdp | rs12527818 |
ensembl | rs12527818 |
geneview | rs12527818 |
scholar | rs12527818 |
rs12527818 | |
pharmgkb | rs12527818 |
gwascentral | rs12527818 |
openSNP | rs12527818 |
23andMe | rs12527818 |
SNPshot | rs12527818 |
SNPdbe | rs12527818 |
MSV3d | rs12527818 |
GWAS Ctlg | rs12527818 |
GMAF | 0.2842 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 0.000007 |
Odds Ratio | 0.2740 None |