Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8048057
rs8048057
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: rs8048210
rs8048210
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: rs8058188
rs8058188
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: rs8203
rs8203
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: rs9923679
rs9923679
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: rs9925228
rs9925228
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: rs9927336
rs9927336
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: rs9927437
rs9927437
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: rs9936903
rs9936903
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: rs9937280
rs9937280
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: rs9940217
rs9940217
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: 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