PCID2, PCI domain containing 2, 55795

N. diseases: 5; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3024739
rs3024739
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34201467
rs34201467
Entrez Id: 55795
Gene Symbol: PCID2
PCID2
CUI: C2985280
Disease:
Blood Protein Measurement
C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs35708060
rs35708060
Entrez Id: 55795
Gene Symbol: PCID2
PCID2
CUI: C2985280
Disease:
Blood Protein Measurement
A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs553316
rs553316
Entrez Id: 55795
Gene Symbol: PCID2
PCID2
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs9549357
rs9549357
Entrez Id: 55795
Gene Symbol: PCID2
PCID2
CUI: C2985280
Disease:
Blood Protein Measurement
A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs3024737
rs3024737
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0037290
Disease:
Skin Pigmentation
G 0.700 GeneticVariation GWASCAT Identification of a novel locus associated with skin colour in African-admixed populations. 28300201 2017
dbSNP: rs61966459
rs61966459
Entrez Id: 55795
Gene Symbol: PCID2
PCID2
CUI: C0524587
Disease:
Mean Corpuscular Volume (result)
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs61966459
rs61966459
Entrez Id: 55795
Gene Symbol: PCID2
PCID2
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs494860
rs494860
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE Our study suggests a functional genetic variation in the PROZ gene, rs494860, may be of importance in bacterial meningitis pathogenesis and cerebral infarction risk. 29746949 2018
dbSNP: rs17882561
rs17882561
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE We studied the distribution of the protein Z gene (rs17882561) (G79A) single-nucleotide polymorphism by PCR-restriction fragment length polymorphism in 100 Egyptian patients with SLE and 100 age, sex, and ethnically matched controls. 26761586 2016
dbSNP: rs3024735
rs3024735
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0002895
Disease:
Anemia, Sickle Cell
0.010 GeneticVariation BEFREE The minor allele frequency of rs3024718 (P=0.03), rs3024719 (P=0.02), rs3024731 (P<0.001), and rs3024735 (P<0.001) were higher in VOC patients than control SCD patients. 22576309 2012
dbSNP: rs3024735
rs3024735
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0750151
Disease:
Vaso-Occlusive Crisis
0.010 GeneticVariation BEFREE Four-locus (rs3024718/rs3024719/rs3024731/rs3024735) PZ haplotypes analysis demonstrated increased frequency of GAAA (P=0.024), AGAA (P=0.011), and GGTG (P=0.002), and reduced frequency of AGTG haplotype (P=0.001) in VOC than in steady-state control patients, thereby conferring disease susceptibility and protective nature to these haplotypes, respectively. 22576309 2012
dbSNP: rs3024772
rs3024772
Entrez Id: 8858;55795
Gene Symbol: PROZ;PCID2
PROZ;PCID2
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE We genotyped 365 pediatric stroke/TE families (stroke n = 216; TE n = 149) for 4 single nucleotide polymorphisms (SNPs; rs3024718, rs3024731, rs3024772, and rs3024778) to assess the association between genetic variation within a conserved block of linkage disequilibrium harboring the PZ gene and pediatric TE. 19050305 2009