PDGFC, platelet derived growth factor C, 56034

N. diseases: 69; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10517653
rs10517653
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10517660
rs10517660
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11100083
rs11100083
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs76488803
rs76488803
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7672622
rs7672622
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs4691380
rs4691380
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs7657225
rs7657225
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs7657225
rs7657225
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs6822892
rs6822892
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs113128512
rs113128512
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4691380
rs4691380
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs4691380
rs4691380
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0005893
Disease:
Body mass index procedure 		T 0.700 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs4691380
rs4691380
Entrez Id: 56034
Gene Symbol: PDGFC
PDGFC
CUI: C0578022
Disease:
Finding of body mass index 		T 0.700 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012