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rs3785982

From SNPedia

Orientationplus
Stabilizedplus
Make rs3785982(C;C)
Make rs3785982(C;T)
Make rs3785982(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position9186907
GeneNTN1
is asnp
is mentioned by
dbSNPrs3785982
ebirs3785982
HLIrs3785982
Exacrs3785982
Varsomers3785982
Maprs3785982
PheGenIrs3785982
hapmaprs3785982
1000 genomesrs3785982
hgdprs3785982
ensemblrs3785982
gopubmedrs3785982
geneviewrs3785982
scholarrs3785982
googlers3785982
pharmgkbrs3785982
gwascentralrs3785982
openSNPrs3785982
23andMers3785982
23andMe allrs3785982
SNP Nexus

SNPshotrs3785982
SNPdbers3785982
MSV3drs3785982
GWAS Ctlgrs3785982
GMAF0.1051
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23319801OA-icon.png]
Trait Breast cancer (prognosis)
Title Identification of Inherited Genetic Variations Influencing Prognosis in Early-Onset Breast Cancer.
Risk Allele
P-val 8E-6
Odds Ratio 1.40 [1.21-1.62]