Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE This study demonstrated a significant association between the MSMB rs10993994 polymorphisms and PCa risk. 31773691

2019

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Overall, none associations between the allelic variants of rs10993994 polymorphisms with whole and PC aggressiveness were found. 30774776

2019

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Our data indicated that MSMB gene rs10993994 polymorphism was associated with an increased risk of PC. 28212531

2017

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
T 0.800 GeneticVariation GWASDB Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies. 24753544

2014

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Rs11672691 and rs10993994 were associated with both fatal and nonfatal PCa, while rs6465657, rs7127900, rs2735839, and rs13385191 were associated with nonfatal PCa only. 24411283

2014

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE BACKGROUND.With recent advances in high-throughput sequencing technologies, many prostate cancer risk loci have been identified, including rs10993994, a single nucleotide polymorphism (SNP) located near the MSMB gene. 24464504

2014

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Regardless of race and ethnicity or rs10993994 genotype, men with low blood levels of MSP have increased risk of prostate cancer. 23213189

2013

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Association of prostate cancer susceptibility variant (MSMB) rs10993994 with risk of spermatogenic failure. 23608167

2013

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE The rs10993994 genotype in the MSMB gene modifies the association between number of sexual partners and PCa risk. 24037734

2013

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE These data indicate that the increase in PC risk associated with rs10993994:C>T is likely mediated by the variant's effect on PSP94 expression; however, this effect does not extend to NCOA4 in the data presented here. 22887727

2013

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE PCa susceptibility was associated with TT genotype of SNP rs10993994 in this cohort of Scottish men and the increased risk of PCa was modified by serum enterolactone concentrations. 22733159

2012

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Six markers associated with early-onset prostate cancer [rs2171492 (7q32), rs6983561 (8q24), rs10993994 (10q11), rs4430796 (17q12), rs1799950 (17q21), and rs266849 (19q13)] were genotyped. 22144497

2012

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Cells with prostate cancer risk alleles at rs10993994 seem to cope more efficiently with DNA double strand breaks (less MN) in a shorter time (decreased MD index). 22677538

2012

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE After allowing for multiple testing, none of the SNPs examined were significantly associated with growth factor or hormone concentrations, and the SNP-prostate cancer associations did not differ by these concentrations, although 4 interactions were marginally significant (MSMB-rs10993994 with androstenedione (uncorrected P = 0.008); CTBP2-rs4962416 with IGFBP-3 (uncorrected P = 0.003); 11q13.2-rs12418451 with IGF-1 (uncorrected P = 0.006); and 11q13.2-rs10896449 with SHBG (uncorrected P = 0.005)). 22459122

2012

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been implicated to be independently associated, with respect to the widely reported SNP rs10993994 in the nearby gene MSMB, with prostate cancer in men of European descent. 20717903

2011

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE The rs10993994 risk allele for prostate cancer results in clinically relevant changes in microseminoprotein-beta expression in tissue and urine. 20967219

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation GWASDB Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. 20676098

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE SNP rs10993994 is 2 bp upstream of the transcription initiation site of MSMB and was identified as an associated PrCa risk variant. 19997100

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Genome-wide association studies (GWAS) have established a variant, rs10993994, on chromosome 10q11 as being associated with prostate cancer risk. 21085629

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Our results suggest a mechanism by which rs10993994 might predispose to prostate cancer and raise the possibility that genetic variation might need to be considered in interpreting the levels of these biomarkers. 20696662

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE rs10993994 in MSMB promoter affects serum MSMB expression, contributes to the genetic predisposition to prostate cancer in southern Chinese Han population. 20333697

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE We examined the association between rs10993994 genotype and MSP levels in a sample of 500 prostate cancer-free men from four racial/ethnic populations in the Multiethnic Cohort (European Americans, African Americans, Latinos, and Japanese Americans). 20736317

2010

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE In conclusion, loci associated with risk for prostate cancer, such as rs7920517 and rs10993994, might also be used to predict the recurrence of prostate-specific antigen in prostate cancer patients receiving radical prostatectomy. 19900942

2009

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Recent functional work has shown that different alleles of the significantly associated SNP in the promoter of MSMB found to be associated with prostate cancer risk, rs10993994, can influence its expression in tumors and in vitro studies. 19644707

2009

dbSNP: rs10993994
rs10993994
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE For the two SNPs that had significant differences between more and less aggressive disease rs2735839 in KLK3 (P = 8.4 x 10(-7)) and rs10993994 in MSMB (P = 0.046), the alleles that are associated with increased risk for PCa were more frequent in patients with less aggressive disease. 19434657

2009