RS137852482 HPRT1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
HPRT LONDON
Lesch-Nyhan syndrome
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
HPRT LONDON
Lesch-Nyhan syndrome
Other Variants in HPRT1