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rs16886165

From SNPedia

Orientationplus
Stabilizedplus
Make rs16886165(G;G)
Make rs16886165(G;T)
Make rs16886165(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position56727256
is asnp
is mentioned by
dbSNPrs16886165
ebirs16886165
HLIrs16886165
Exacrs16886165
Varsomers16886165
Maprs16886165
PheGenIrs16886165
hapmaprs16886165
1000 genomesrs16886165
hgdprs16886165
ensemblrs16886165
gopubmedrs16886165
geneviewrs16886165
scholarrs16886165
googlers16886165
pharmgkbrs16886165
gwascentralrs16886165
openSNPrs16886165
23andMers16886165
23andMe allrs16886165
SNP Nexus

SNPshotrs16886165
SNPdbers16886165
MSV3drs16886165
GWAS Ctlgrs16886165
GMAF0.2383
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19330030OA-icon.png]
Trait Breast cancer
Title A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
Risk Allele G
P-val 5E-7
Odds Ratio



[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


GET Evidence
rs16886165
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary



[PMID 22965832] Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population.