RS554675432 PROK2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypogonadotropic hypogonadism 4 with or without anosmia
PROK2-related disorder
Inborn genetic diseases
Male infertility with azoospermia or oligozoospermia due to single gene mutation
Hypogonadotropic hypogonadism 4 with or without anosmia
PROK2-related disorder
Inborn genetic diseases
Male infertility with azoospermia or oligozoospermia due to single gene mutation
Other Variants in PROK2