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rs4784227

From SNPedia

Orientationplus
Stabilizedplus
Make rs4784227(C;C)
Make rs4784227(C;T)
Make rs4784227(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position52565276
GenePLSCR3
is asnp
is mentioned by
dbSNPrs4784227
ebirs4784227
HLIrs4784227
Exacrs4784227
Varsomers4784227
Maprs4784227
PheGenIrs4784227
hapmaprs4784227
1000 genomesrs4784227
hgdprs4784227
ensemblrs4784227
gopubmedrs4784227
geneviewrs4784227
scholarrs4784227
googlers4784227
pharmgkbrs4784227
gwascentralrs4784227
openSNPrs4784227
23andMers4784227
23andMe allrs4784227
SNP Nexus

SNPshotrs4784227
SNPdbers4784227
MSV3drs4784227
GWAS Ctlgrs4784227
GMAF0.2181
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20585626OA-icon.png] Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia breast cancer consortium

The adjusted odds ratio for breast cancer risk was 1.25 (CI: 1.20?1.31) per rs4784227(T) allele (p = 3.2×10e?25) in the pooled analysis of of over 10,000 samples from all Asian samples, and 1.19 (CI: 1.09-1.31, p = 1.3x10e-4) among European Americans (2,797 cases and 2,662 controls).


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


[PMID 22452962OA-icon.png] A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study


[PMID 23001124OA-icon.png] Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression.


[PMID 25995231] ABC: A tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments