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rs1011970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1011970(G;T)
Make rs1011970(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22062135
GeneCDKN2B-AS1, LOC102724137
is asnp
is mentioned by
dbSNPrs1011970
ebirs1011970
HLIrs1011970
Exacrs1011970
Varsomers1011970
Maprs1011970
PheGenIrs1011970
hapmaprs1011970
1000 genomesrs1011970
hgdprs1011970
ensemblrs1011970
gopubmedrs1011970
geneviewrs1011970
scholarrs1011970
googlers1011970
pharmgkbrs1011970
gwascentralrs1011970
openSNPrs1011970
23andMers1011970
23andMe allrs1011970
SNP Nexus

SNPshotrs1011970
SNPdbers1011970
MSV3drs1011970
GWAS Ctlgrs1011970
GMAF0.2208
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20453838OA-icon.png]
Trait Breast cancer
Title Genome-wide association study identifies five new breast cancer susceptibility loci
Risk Allele T
P-val 3E-8
Odds Ratio 1.09 [1.04-1.14]


[PMID 21445572] Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies


[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 19686382OA-icon.png] Genome-wide associations studies for melanoma and nevi.


[PMID 20386740OA-icon.png] Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.


[PMID 22198471] Genetic variants at chromosome 9p21, 10p15 and 10q22 and breast cancer susceptibility in a Chinese population.


[PMID 22461340OA-icon.png] 11q13 is a susceptibility locus for hormone receptor positive breast cancer

[PMID 22198471] in Chinese women no significant breast cancer association at rs1011970, rs10757278 or rs2380205

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 6E-8
Odds Ratio 1.06 [1.03-1.08]


[PMID 26070784] Genetic risk variants associated with in situ breast cancer


[PMID 26248686] Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy