Have questions? Visit https://www.reddit.com/r/SNPedia

rs865686

From SNPedia

Orientationplus
Stabilizedplus
Make rs865686(G;G)
Make rs865686(G;T)
Make rs865686(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position108126198
is asnp
is mentioned by
dbSNPrs865686
ebirs865686
HLIrs865686
Exacrs865686
Varsomers865686
Maprs865686
PheGenIrs865686
hapmaprs865686
1000 genomesrs865686
hgdprs865686
ensemblrs865686
gopubmedrs865686
geneviewrs865686
scholarrs865686
googlers865686
pharmgkbrs865686
gwascentralrs865686
openSNPrs865686
23andMers865686
23andMe allrs865686
SNP Nexus

SNPshotrs865686
SNPdbers865686
MSV3drs865686
GWAS Ctlgrs865686
GMAF0.3191
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 21263130] Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study


[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 22859399OA-icon.png] 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

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 T
P-val 1E-34
Odds Ratio 1.12 [1.1-1.14]


[PMID 25002657] Breast cancer susceptibility variants and mammographic density phenotypes in Norwegian postmenopausal women


[PMID 25652398OA-icon.png] Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2