rs3129860
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3129860(A;A) |
Make rs3129860(A;G) |
Make rs3129860(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32433302 |
is a | snp |
is | mentioned by |
dbSNP | rs3129860 |
dbSNP (classic) | rs3129860 |
ClinGen | rs3129860 |
ebi | rs3129860 |
HLI | rs3129860 |
Exac | rs3129860 |
Gnomad | rs3129860 |
Varsome | rs3129860 |
LitVar | rs3129860 |
Map | rs3129860 |
PheGenI | rs3129860 |
Biobank | rs3129860 |
1000 genomes | rs3129860 |
hgdp | rs3129860 |
ensembl | rs3129860 |
geneview | rs3129860 |
scholar | rs3129860 |
rs3129860 | |
pharmgkb | rs3129860 |
gwascentral | rs3129860 |
openSNP | rs3129860 |
23andMe | rs3129860 |
SNPshot | rs3129860 |
SNPdbe | rs3129860 |
MSV3d | rs3129860 |
GWAS Ctlg | rs3129860 |
GMAF | 0.09734 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23321320] |
Trait | Hepatitis C induced liver cirrhosis |
Title | A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region. |
Risk Allele | A |
P-val | 1E-9 |
Odds Ratio | 1.36 [1.22-1.49] |
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
[PMID 21379322] Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.