Have questions? Visit https://www.reddit.com/r/SNPedia

rs2952155

From SNPedia

Orientationplus
Stabilizedplus
Make rs2952155(C;C)
Make rs2952155(C;T)
Make rs2952155(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position39705465
GeneERBB2
is asnp
is mentioned by
dbSNPrs2952155
ebirs2952155
HLIrs2952155
Exacrs2952155
Varsomers2952155
Maprs2952155
PheGenIrs2952155
hapmaprs2952155
1000 genomesrs2952155
hgdprs2952155
ensemblrs2952155
gopubmedrs2952155
geneviewrs2952155
scholarrs2952155
googlers2952155
pharmgkbrs2952155
gwascentralrs2952155
openSNPrs2952155
23andMers2952155
23andMe allrs2952155
SNP Nexus

SNPshotrs2952155
SNPdbers2952155
MSV3drs2952155
GWAS Ctlgrs2952155
GMAF0.3664
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 17132159OA-icon.png] Comprehensive analysis of the ATM, CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study.

[PMID 19240718OA-icon.png] Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer.


GET Evidence
rs2952155
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.68254
summary