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rs345013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs345013(C;C)
Make rs345013(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position145456001
is asnp
is mentioned by
dbSNPrs345013
ebirs345013
HLIrs345013
Exacrs345013
Varsomers345013
Maprs345013
PheGenIrs345013
hapmaprs345013
1000 genomesrs345013
hgdprs345013
ensemblrs345013
gopubmedrs345013
geneviewrs345013
scholarrs345013
googlers345013
pharmgkbrs345013
gwascentralrs345013
openSNPrs345013
23andMers345013
23andMe allrs345013
SNP Nexus

SNPshotrs345013
SNPdbers345013
MSV3drs345013
GWAS Ctlgrs345013
GMAF0.1102
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs345013
PubMedID [PMID 17903305OA-icon.png]
Condition Prostate cancer
Gene Intergenic
Risk Allele
pValue 5.00E-006
OR NA
95% CI



GET Evidence
rs345013
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary