Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1367215622
rs1367215622
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0279680
Disease:
Transitional cell carcinoma of bladder
0.010 GeneticVariation BEFREE Stable <i>TMCO1</i> (wild-type) overexpression suppressed, whereas T33A and S60A mutants recovered, tumor size in xenograft mice.<b>Conclusions:</b> Clinical associations, xenograft mice, and <i>in vitro</i> indications provide solid evidence that the <i>TMCO1</i> gene is a novel tumor suppressor in UBUCs. 28972042 2017
dbSNP: rs1367215622
rs1367215622
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Stable <i>TMCO1</i> (wild-type) overexpression suppressed, whereas T33A and S60A mutants recovered, tumor size in xenograft mice.<b>Conclusions:</b> Clinical associations, xenograft mice, and <i>in vitro</i> indications provide solid evidence that the <i>TMCO1</i> gene is a novel tumor suppressor in UBUCs. 28972042 2017
dbSNP: rs12051443
rs12051443
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0600139
Disease:
Prostate carcinoma
A 0.700 GeneticVariation GWASCAT A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer. 25217961 2014
dbSNP: rs1035545
rs1035545
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs10500559
rs10500559
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs1058747
rs1058747
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs11648674
rs11648674
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs12597065
rs12597065
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs12926987
rs12926987
Entrez Id: 23035;100379141
Gene Symbol: PHLPP2;SNORA70D
PHLPP2;SNORA70D
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs1582589
rs1582589
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs2303224
rs2303224
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs2303225
rs2303225
Entrez Id: 23035;91862
Gene Symbol: PHLPP2;MARVELD3
PHLPP2;MARVELD3
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs28582831
rs28582831
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs34734042
rs34734042
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs35131351
rs35131351
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs3752681
rs3752681
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs3925658
rs3925658
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs4788549
rs4788549
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs4788826
rs4788826
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs4788827
rs4788827
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs60881203
rs60881203
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs61733124
rs61733124
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs61733125
rs61733125
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs62053107
rs62053107
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012
dbSNP: rs62053108
rs62053108
Entrez Id: 23035
Gene Symbol: PHLPP2
PHLPP2
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012