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rs1801201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1801201(A;G)
Make rs1801201(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position39723332
GeneERBB2
is asnp
is mentioned by
dbSNPrs1801201
ebirs1801201
HLIrs1801201
Exacrs1801201
Varsomers1801201
Maprs1801201
PheGenIrs1801201
hapmaprs1801201
1000 genomesrs1801201
hgdprs1801201
ensemblrs1801201
gopubmedrs1801201
geneviewrs1801201
scholarrs1801201
googlers1801201
pharmgkbrs1801201
gwascentralrs1801201
openSNPrs1801201
23andMers1801201
23andMe allrs1801201
SNP Nexus

SNPshotrs1801201
SNPdbers1801201
MSV3drs1801201
GWAS Ctlgrs1801201
GMAF0.002755
Max Magnitude0
OMIM164870
Desc
Variant0002
Relatedalso


ClinVar
Risk rs1801201(C,G;C,G)
Alt rs1801201(C,G;C,G)
Reference rs1801201(A;A)
Significance Non-pathogenic
Disease ERBB2 POLYMORPHISM not specified
Variation info
Gene ERBB2
CLNDBN ERBB2 POLYMORPHISM not specified
Reversed 0
HGVS NC_000017.10:g.37879585A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014888.2, RCV000120743.1,



[PMID 19124506OA-icon.png] Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.


[PMID 19336545OA-icon.png] Heritable variation of ERBB2 and breast cancer risk.