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rs2180341

From SNPedia

Orientationplus
Stabilizedplus
Make rs2180341(A;A)
Make rs2180341(A;G)
Make rs2180341(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position127279485
GeneRNF146
is asnp
is mentioned by
dbSNPrs2180341
dbSNP (classic)rs2180341
ClinGenrs2180341
ebirs2180341
HLIrs2180341
Exacrs2180341
Gnomadrs2180341
Varsomers2180341
LitVarrs2180341
Maprs2180341
PheGenIrs2180341
Biobankrs2180341
1000 genomesrs2180341
hgdprs2180341
ensemblrs2180341
geneviewrs2180341
scholarrs2180341
googlers2180341
pharmgkbrs2180341
gwascentralrs2180341
openSNPrs2180341
23andMers2180341
SNPshotrs2180341
SNPdbers2180341
MSV3drs2180341
GWAS Ctlgrs2180341
GMAF0.2608
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS
SNP rs2180341
PubMedID [PMID 18326623OA-icon.png]
Condition Breast cancer
Gene ECHDC1,RNF146
Risk Allele G
pValue 3.00E-008
OR 1.41
95% CI 1.25-1.59



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


[PMID 21791674OA-icon.png] Interactions Between Genetic Variants and Breast Cancer Risk Factors in the Breast and Prostate Cancer Cohort Consortium


[PMID 19219042OA-icon.png] Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.


[PMID 19330030OA-icon.png] A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).


[PMID 19690183OA-icon.png] The 6q22.33 locus and breast cancer susceptibility.


[PMID 20085711OA-icon.png] Leveraging genetic variability across populations for the identification of causal variants.



[PMID 22269215OA-icon.png] Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women