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rs1810132

From SNPedia

Orientationplus
Stabilizedplus
Make rs1810132(C;C)
Make rs1810132(C;T)
Make rs1810132(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position39709752
GeneERBB2
is asnp
is mentioned by
dbSNPrs1810132
ebirs1810132
HLIrs1810132
Exacrs1810132
Varsomers1810132
Maprs1810132
PheGenIrs1810132
hapmaprs1810132
1000 genomesrs1810132
hgdprs1810132
ensemblrs1810132
gopubmedrs1810132
geneviewrs1810132
scholarrs1810132
googlers1810132
pharmgkbrs1810132
gwascentralrs1810132
openSNPrs1810132
23andMers1810132
23andMe allrs1810132
SNP Nexus

SNPshotrs1810132
SNPdbers1810132
MSV3drs1810132
GWAS Ctlgrs1810132
GMAF0.4146
Max Magnitude
? (C;C) (C;T) (T;T) 28

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



[PMID 18978678OA-icon.png] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.


GET Evidence
rs1810132
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.642239
summary