rs2180341
Orientation | plus |
Stabilized | plus |
Make rs2180341(A;A) |
Make rs2180341(A;G) |
Make rs2180341(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 127279485 |
Gene | RNF146 |
is a | snp |
is | mentioned by |
dbSNP | rs2180341 |
dbSNP (classic) | rs2180341 |
ClinGen | rs2180341 |
ebi | rs2180341 |
HLI | rs2180341 |
Exac | rs2180341 |
Gnomad | rs2180341 |
Varsome | rs2180341 |
LitVar | rs2180341 |
Map | rs2180341 |
PheGenI | rs2180341 |
Biobank | rs2180341 |
1000 genomes | rs2180341 |
hgdp | rs2180341 |
ensembl | rs2180341 |
geneview | rs2180341 |
scholar | rs2180341 |
rs2180341 | |
pharmgkb | rs2180341 |
gwascentral | rs2180341 |
openSNP | rs2180341 |
23andMe | rs2180341 |
SNPshot | rs2180341 |
SNPdbe | rs2180341 |
MSV3d | rs2180341 |
GWAS Ctlg | rs2180341 |
GMAF | 0.2608 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs2180341 |
PubMedID | [PMID 18326623] |
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 21791674] Interactions Between Genetic Variants and Breast Cancer Risk Factors in the Breast and Prostate Cancer Cohort Consortium
[PMID 19219042] Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.
[PMID 19330030] 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 20085711] Leveraging genetic variability across populations for the identification of causal variants.
[PMID 22269215] Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women