rs188140481
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
Make rs188140481(A;A) |
Make rs188140481(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 127179427 |
is a | snp |
is | mentioned by |
dbSNP | rs188140481 |
dbSNP (classic) | rs188140481 |
ClinGen | rs188140481 |
ebi | rs188140481 |
HLI | rs188140481 |
Exac | rs188140481 |
Gnomad | rs188140481 |
Varsome | rs188140481 |
LitVar | rs188140481 |
Map | rs188140481 |
PheGenI | rs188140481 |
Biobank | rs188140481 |
1000 genomes | rs188140481 |
hgdp | rs188140481 |
ensembl | rs188140481 |
geneview | rs188140481 |
scholar | rs188140481 |
rs188140481 | |
pharmgkb | rs188140481 |
gwascentral | rs188140481 |
openSNP | rs188140481 |
23andMe | rs188140481 |
SNPshot | rs188140481 |
SNPdbe | rs188140481 |
MSV3d | rs188140481 |
GWAS Ctlg | rs188140481 |
Max Magnitude | 0 |
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 24952954] 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 27262462] Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.