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rs10822013

From SNPedia

Orientationplus
Stabilizedplus
Make rs10822013(C;C)
Make rs10822013(C;T)
Make rs10822013(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position62492218
GeneZNF365
is asnp
is mentioned by
dbSNPrs10822013
dbSNP (classic)rs10822013
ClinGenrs10822013
ebirs10822013
HLIrs10822013
Exacrs10822013
Gnomadrs10822013
Varsomers10822013
LitVarrs10822013
Maprs10822013
PheGenIrs10822013
Biobankrs10822013
1000 genomesrs10822013
hgdprs10822013
ensemblrs10822013
geneviewrs10822013
scholarrs10822013
googlers10822013
pharmgkbrs10822013
gwascentralrs10822013
openSNPrs10822013
23andMers10822013
SNPshotrs10822013
SNPdbers10822013
MSV3drs10822013
GWAS Ctlgrs10822013
GMAF0.4197
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21908515OA-icon.png]
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 27863437OA-icon.png] Association of multiple genetic variants with breast cancer susceptibility in the Han Chinese population.