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rs2380205

From SNPedia

Orientationplus
Stabilizedplus
Make rs2380205(C;C)
Make rs2380205(C;T)
Make rs2380205(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position5844771
is asnp
is mentioned by
dbSNPrs2380205
ebirs2380205
HLIrs2380205
Exacrs2380205
Varsomers2380205
Maprs2380205
PheGenIrs2380205
hapmaprs2380205
1000 genomesrs2380205
hgdprs2380205
ensemblrs2380205
gopubmedrs2380205
geneviewrs2380205
scholarrs2380205
googlers2380205
pharmgkbrs2380205
gwascentralrs2380205
openSNPrs2380205
23andMers2380205
23andMe allrs2380205
SNP Nexus

SNPshotrs2380205
SNPdbers2380205
MSV3drs2380205
GWAS Ctlgrs2380205
GMAF0.3825
Max Magnitude
? (C;C) (C;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 C
P-val 5E-7
Odds Ratio 1.06 [1.02-1.10]


[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 22198471] Genetic variants at chromosome 9p21, 10p15 and 10q22 and breast cancer susceptibility in a Chinese population. four common SNPs at 9p21(rs1011970 and rs10757278), 10p15 (rs2380205), and 10q22 (rs1250009) in a two-stage case-control study with a total of 1792 breast cancer cases and 1,867 controls. We found that rs1250009 at 10q22 was consistently associated with risk of breast cancer in stage 1 and stage 2, with a per-allele OR of 1.13 (95% CI 1.02-1.25) after two stages combined (P = 0.023). However, no significant associations were observed between the other three SNPs and breast cancer risk.


[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


[PMID 26175953OA-icon.png] FGFR2 gene polymorphisms are associated with breast cancer risk in the Han Chinese population