RS137852490 HPRT1

Health Risk Chr X:134500030
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
Other Variants in HPRT1
rs137852477 rs137852478 rs137852479 rs2077615673 rs137852480 rs387906428 rs137852481 rs267606863 rs137852482 rs2520840422
Ask Dr. Hemsworth about this variant