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rs11228565

From SNPedia

Orientationplus
Stabilizedplus
Make rs11228565(A;A)
Make rs11228565(A;G)
Make rs11228565(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69211113
is asnp
is mentioned by
dbSNPrs11228565
ebirs11228565
HLIrs11228565
Exacrs11228565
Varsomers11228565
Maprs11228565
PheGenIrs11228565
hapmaprs11228565
1000 genomesrs11228565
hgdprs11228565
ensemblrs11228565
gopubmedrs11228565
geneviewrs11228565
scholarrs11228565
googlers11228565
pharmgkbrs11228565
gwascentralrs11228565
openSNPrs11228565
23andMers11228565
23andMe allrs11228565
SNP Nexus

SNPshotrs11228565
SNPdbers11228565
MSV3drs11228565
GWAS Ctlgrs11228565
GMAF0.1226
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19767754OA-icon.png] Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
OMIM611958
Desc
Variant
Relatedalso
[PMID 22077888OA-icon.png] Association of prostate cancer risk alleles with unfavourable pathological characteristics in potential candidates for active surveillance.


[PMID 22468268OA-icon.png] Comprehensive resequence analysis of a 123-kb region of chromosome 11q13 associated with prostate cancer.


GET Evidence
rs11228565
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary



[PMID 24037955] The presence of prostate cancer at biopsy is predicted by a number of genetic variants