Variant: rs1077989 

    present in Gene: GPHN;TMEM229B
    present in Chromosome: 14
    Position on Chromosome: 67509105
    Alleles of this Variant: A/C

rs1077989 in GPHN;TMEM229B gene and Chronic Kidney Diseases PMID 29545352 2018 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.

rs1077989 in GPHN;TMEM229B gene and Kidney Failure, Chronic PMID 29545352 2018 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.

rs1077989 in GPHN;TMEM229B gene and Phospholipid measurement PMID 22359512 2012 Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.