Variant: rs145591298 

    present in Gene: CLDN19
    present in Chromosome: 1
    Position on Chromosome: 42735969
    Alleles of this Variant: C/T

rs145591298 in CLDN19 gene and Nephrocalcinosis PMID 28893421 2018 Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.

rs145591298 in CLDN19 gene and Nephrolithiasis PMID 28893421 2018 Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.