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rs10934853

From SNPedia

Orientationplus
Stabilizedplus
Make rs10934853(A;A)
Make rs10934853(A;C)
Make rs10934853(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position128319530
GeneEEFSEC
is asnp
is mentioned by
dbSNPrs10934853
ebirs10934853
HLIrs10934853
Exacrs10934853
Varsomers10934853
Maprs10934853
PheGenIrs10934853
hapmaprs10934853
1000 genomesrs10934853
hgdprs10934853
ensemblrs10934853
gopubmedrs10934853
geneviewrs10934853
scholarrs10934853
googlers10934853
pharmgkbrs10934853
gwascentralrs10934853
openSNPrs10934853
23andMers10934853
23andMe allrs10934853
SNP Nexus

SNPshotrs10934853
SNPdbers10934853
MSV3drs10934853
GWAS Ctlgrs10934853
GMAF0.4513
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 19767754OA-icon.png] Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
OMIM176807
Desc
Variant
Relatedalso


[PMID 21898988] [Two single nucleotide polymorphisms on chromosome 3 and the risk of prostate cancer in Chinese men] rs10934853 and rs2660753 on chromosome 3 are not obviously correlated with PCa in Chinese patients


[PMID 22077888OA-icon.png] Association of prostate cancer risk alleles with unfavourable pathological characteristics in potential candidates for active surveillance.


GET Evidence
rs10934853
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary