rs10771399
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10771399(A;A) |
Make rs10771399(A;G) |
Make rs10771399(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 28002147 |
is a | snp |
is | mentioned by |
dbSNP | rs10771399 |
dbSNP (classic) | rs10771399 |
ClinGen | rs10771399 |
ebi | rs10771399 |
HLI | rs10771399 |
Exac | rs10771399 |
Gnomad | rs10771399 |
Varsome | rs10771399 |
LitVar | rs10771399 |
Map | rs10771399 |
PheGenI | rs10771399 |
Biobank | rs10771399 |
1000 genomes | rs10771399 |
hgdp | rs10771399 |
ensembl | rs10771399 |
geneview | rs10771399 |
scholar | rs10771399 |
rs10771399 | |
pharmgkb | rs10771399 |
gwascentral | rs10771399 |
openSNP | rs10771399 |
23andMe | rs10771399 |
SNPshot | rs10771399 |
SNPdbe | rs10771399 |
MSV3d | rs10771399 |
GWAS Ctlg | rs10771399 |
GMAF | 0.1019 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22348646] Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
[PMID 22267197] Genome-wide association analysis identifies three new breast cancer susceptibility loci
GWAS snp | |
---|---|
PMID | [PMID 23544013] |
Trait | Breast Cancer in BRCA1 mutation carriers |
Title | Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | 1.18 [1.1-1.27] |
GWAS snp | |
---|---|
PMID | [PMID 23535733] |
Trait | Breast cancer |
Title | Genome-wide association studies identify four ER negative-specific breast cancer risk loci. |
Risk Allele | T |
P-val | 2E-12 |
Odds Ratio | 1.20 [1.15-1.27] |
GWAS snp | |
---|---|
PMID | [PMID 23535729] |
Trait | Breast cancer |
Title | Large-scale genotyping identifies 41 new loci associated with breast cancer risk. |
Risk Allele | A |
P-val | 8E-31 |
Odds Ratio | 1.16 [1.14-1.2] |
GWAS snp | |
---|---|
PMID | [PMID 24325915] |
Trait | Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) |
Title | Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. |
Risk Allele | G |
P-val | 2E-8 |
Odds Ratio | 1.39 [1.25-1.56] |
[PMID 27459855] Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.