PIGR, polymeric immunoglobulin receptor, 5284

N. diseases: 71; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2007272
rs2007272
Entrez Id: 5284
Gene Symbol: PIGR
PIGR
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs2007272
rs2007272
Entrez Id: 5284
Gene Symbol: PIGR
PIGR
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs291091
rs291091
Entrez Id: 5284
Gene Symbol: PIGR
PIGR
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs4844555
rs4844555
Entrez Id: 5284
Gene Symbol: PIGR
PIGR
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2275531
rs2275531
Entrez Id: 5284
Gene Symbol: PIGR
PIGR
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.010 GeneticVariation BEFREE Haplotype of the two missense PIGR SNPs, 1093G-->A and 1739C-->T, and sequence analyses have confirmed the role of the nucleotide PIGR1739 and excluded possibility of an additional significant nonsynonymous NPC susceptibility SNP. 12546713 2003
dbSNP: rs291102
rs291102
Entrez Id: 5284
Gene Symbol: PIGR
PIGR
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.010 GeneticVariation BEFREE Haplotype of the two missense PIGR SNPs, 1093G-->A and 1739C-->T, and sequence analyses have confirmed the role of the nucleotide PIGR1739 and excluded possibility of an additional significant nonsynonymous NPC susceptibility SNP. 12546713 2003