Rs2180341

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Orientationplus
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
Exacrs2180341
PheGenIrs2180341
nextbiors2180341
hapmaprs2180341
1000 genomesrs2180341
hgdprs2180341
ensemblrs2180341
gopubmedrs2180341
geneviewrs2180341
scholarrs2180341
googlers2180341
pharmgkbrs2180341
gwascentralrs2180341
openSNPrs2180341
23andMers2180341
23andMe allrs2180341
SNP Nexus

SNPshotrs2180341
SNPdbers2180341
MSV3drs2180341
GMAF0.2608
? (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 19690183] The 6q22.33 locus and breast cancer susceptibility.


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


GET Evidence
rs2180341
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.789062
summary



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