RS794727238 HPRT1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
HPRT1-related disorder
Nephrolithiasis/nephrocalcinosis
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
HPRT1-related disorder
Nephrolithiasis/nephrocalcinosis
Other Variants in HPRT1