rs9977253
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9977253(C;C) |
Make rs9977253(C;T) |
Make rs9977253(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 25272769 |
is a | snp |
is | mentioned by |
dbSNP | rs9977253 |
dbSNP (classic) | rs9977253 |
ClinGen | rs9977253 |
ebi | rs9977253 |
HLI | rs9977253 |
Exac | rs9977253 |
Gnomad | rs9977253 |
Varsome | rs9977253 |
LitVar | rs9977253 |
Map | rs9977253 |
PheGenI | rs9977253 |
Biobank | rs9977253 |
1000 genomes | rs9977253 |
hgdp | rs9977253 |
ensembl | rs9977253 |
geneview | rs9977253 |
scholar | rs9977253 |
rs9977253 | |
pharmgkb | rs9977253 |
gwascentral | rs9977253 |
openSNP | rs9977253 |
23andMe | rs9977253 |
SNPshot | rs9977253 |
SNPdbe | rs9977253 |
MSV3d | rs9977253 |
GWAS Ctlg | rs9977253 |
GMAF | 0.1671 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20708005] |
Trait | |
Title | Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease |
Risk Allele | G |
P-val | 0.000005 |
Odds Ratio | 0.76 [NR] unit increase |