Table 2 - Identification of modifier gene variants overrepresented in familial hypomagnesemia with hypercalciuria and nephrocalcinosis patients with a more aggressive renal phenotype

Comparison of the genotype distribution obtained by Open Array genotyping data in the validation cohort and by whole exome sequencing data from the discovery cohort.Data from the three possible genotypes is shown for each candidate modifier gene variant across the two FHHNC renal phenotypes (FAST and noFAST), the healthy control cohort and the control group from GTEx.