rs130067
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs130067(A;C) |
Make rs130067(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31150734 |
Gene | CCHCR1 |
is a | snp |
is | mentioned by |
dbSNP | rs130067 |
dbSNP (classic) | rs130067 |
ClinGen | rs130067 |
ebi | rs130067 |
HLI | rs130067 |
Exac | rs130067 |
Gnomad | rs130067 |
Varsome | rs130067 |
LitVar | rs130067 |
Map | rs130067 |
PheGenI | rs130067 |
Biobank | rs130067 |
1000 genomes | rs130067 |
hgdp | rs130067 |
ensembl | rs130067 |
geneview | rs130067 |
scholar | rs130067 |
rs130067 | |
pharmgkb | rs130067 |
gwascentral | rs130067 |
openSNP | rs130067 |
23andMe | rs130067 |
SNPshot | rs130067 |
SNPdbe | rs130067 |
MSV3d | rs130067 |
GWAS Ctlg | rs130067 |
GMAF | 0.2447 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21743467] |
Trait | |
Title | Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. |
Risk Allele | G |
P-val | 3E-8 |
Odds Ratio | 1.0500 [1.02-1.09] |
[PMID 22985493] Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis.