Variant: rs498872 

    present in Gene: PHLDB1
    present in Chromosome: 11
    Position on Chromosome: 118606652
    Alleles of this Variant: A/G;T

rs498872 in PHLDB1 gene and Central Nervous System Neoplasms PMID 19578367 2009 Genome-wide association study identifies five susceptibility loci for glioma.

PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.

rs498872 in PHLDB1 gene and Glioma PMID 19578367 2009 We identified five risk loci for glioma at 5p15.33 (rs2736100, TERT; P = 1.50 x 10(-17)), 8q24.21 (rs4295627, CCDC26; P = 2.34 x 10(-18)), 9p21.3 (rs4977756, CDKN2A-CDKN2B; P = 7.24 x 10(-15)), 20q13.33 (rs6010620, RTEL1; P = 2.52 x 10(-12)) and 11q23.3 (rs498872, PHLDB1; P = 1.07 x 10(-8)).

PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.

PMID 30714141 2019 Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility.

rs498872 in PHLDB1 gene and Nasopharyngeal carcinoma PMID 20512145 2010 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.