Variant: rs757796926 

    present in Gene: GRHPR
    present in Chromosome: 9
    Position on Chromosome: 37426659
    Alleles of this Variant: G/A

rs757796926 in GRHPR gene and Nephrocalcinosis PMID 28893421 2018 Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.

rs757796926 in GRHPR gene and Nephrolithiasis PMID 28893421 2018 Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.