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rs188140481

From SNPedia

Orientationplus
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ReferenceGRCh38 38.1/141
Chromosome8
Position127179427
is asnp
is mentioned by
dbSNPrs188140481
dbSNP (old)rs188140481
ClinGenrs188140481
ebirs188140481
HLIrs188140481
Exacrs188140481
Gnomadrs188140481
Varsomers188140481
Maprs188140481
PheGenIrs188140481
Biobankrs188140481
1000 genomesrs188140481
hgdprs188140481
ensemblrs188140481
gopubmedrs188140481
geneviewrs188140481
scholarrs188140481
googlers188140481
pharmgkbrs188140481
gwascentralrs188140481
openSNPrs188140481
23andMers188140481
23andMe allrs188140481
SNP Nexus

SNPshotrs188140481
SNPdbers188140481
MSV3drs188140481
GWAS Ctlgrs188140481
Max Magnitude

This SNP may be most notable for being a perfect proxy for rs138042437; both are considered markers for a haplotype associated with moderately increased risk for prostate cancer.


[PMID 24952954OA-icon.png] A Rare 8q24 SNP Predisposes North American Men to Prostate Cancer and Possibly More Aggressive Disease

[PMID 25187206] The variant allele of the rs188140481 polymorphism confers a moderate increase in the risk of prostate cancer in Polish men [PMID 27262462OA-icon.png] Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.