rs10822013
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10822013(C;C) |
Make rs10822013(C;T) |
Make rs10822013(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 62492218 |
Gene | ZNF365 |
is a | snp |
is | mentioned by |
dbSNP | rs10822013 |
dbSNP (classic) | rs10822013 |
ClinGen | rs10822013 |
ebi | rs10822013 |
HLI | rs10822013 |
Exac | rs10822013 |
Gnomad | rs10822013 |
Varsome | rs10822013 |
LitVar | rs10822013 |
Map | rs10822013 |
PheGenI | rs10822013 |
Biobank | rs10822013 |
1000 genomes | rs10822013 |
hgdp | rs10822013 |
ensembl | rs10822013 |
geneview | rs10822013 |
scholar | rs10822013 |
rs10822013 | |
pharmgkb | rs10822013 |
gwascentral | rs10822013 |
openSNP | rs10822013 |
23andMe | rs10822013 |
SNPshot | rs10822013 |
SNPdbe | rs10822013 |
MSV3d | rs10822013 |
GWAS Ctlg | rs10822013 |
GMAF | 0.4197 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21908515] |
Trait | |
Title | Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium. |
Risk Allele | T |
P-val | 6E-9 |
Odds Ratio | 1.1200 [1.06-1.18] |
[PMID 27863437] Association of multiple genetic variants with breast cancer susceptibility in the Han Chinese population.