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rs1058808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1058808(C;G)
Make rs1058808(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position39727784
GeneERBB2
is asnp
is mentioned by
dbSNPrs1058808
ebirs1058808
HLIrs1058808
Exacrs1058808
Varsomers1058808
Maprs1058808
PheGenIrs1058808
hapmaprs1058808
1000 genomesrs1058808
hgdprs1058808
ensemblrs1058808
gopubmedrs1058808
geneviewrs1058808
scholarrs1058808
googlers1058808
pharmgkbrs1058808
gwascentralrs1058808
openSNPrs1058808
23andMers1058808
23andMe allrs1058808
SNP Nexus

SNPshotrs1058808
SNPdbers1058808
MSV3drs1058808
GWAS Ctlgrs1058808
GMAF0.4908
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 19438491] The effects of obesity and HER-2 polymorphisms as risk factors for endometrial cancer in Korean women

[PMID 17267408OA-icon.png] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.

[PMID 17598910OA-icon.png] Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia.

[PMID 19055823OA-icon.png] The genetic polymorphisms of HER-2 and the risk of lung cancer in a Korean population.

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

GET Evidence
ERBB2-P1170A
aa_change Pro1170Ala
aa_change_short P1170A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.511528
summary



[PMID 23200760] Pathway analysis of genome-wide association study on asthma

ClinVar
Risk rs1058808(G;G)
Alt rs1058808(G;G)
Reference rs1058808(C;C)
Significance Untested
Disease not specified
Variation info
Gene ERBB2
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.37884037C>G
CLNSRC ClinVar
CLNACC RCV000120753.1,



[PMID 26323365] Effects of HER2 genetic polymorphisms on its protein expression in breast cancer