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rs10771399

From SNPedia

Orientationminus
Stabilizedplus
Make rs10771399(A;A)
Make rs10771399(A;G)
Make rs10771399(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position28155080
is asnp
is mentioned by
dbSNPrs10771399
ebirs10771399
HLIrs10771399
Exacrs10771399
Varsomers10771399
Maprs10771399
PheGenIrs10771399
hapmaprs10771399
1000 genomesrs10771399
hgdprs10771399
ensemblrs10771399
gopubmedrs10771399
geneviewrs10771399
scholarrs10771399
googlers10771399
pharmgkbrs10771399
gwascentralrs10771399
openSNPrs10771399
23andMers10771399
23andMe allrs10771399
SNP Nexus

SNPshotrs10771399
SNPdbers10771399
MSV3drs10771399
GWAS Ctlgrs10771399
GMAF0.1019
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22348646OA-icon.png] 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 22267197OA-icon.png] Genome-wide association analysis identifies three new breast cancer susceptibility loci

GWAS snp
PMID [PMID 23544013OA-icon.png]
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 23535733OA-icon.png]
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 23535729OA-icon.png]
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 24325915OA-icon.png]
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.