Related gene-specific medical variations for Gene (Select 60675) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3248550	NM_001126128.2(PROK2):c.96+2T>C	PROK2	Single nucleotide variant (splice donor variant)	Hypogonadotropic hypogonadism	GUncertain significance
Select item 1807454	NM_001126128.2(PROK2):c.57G>C (p.Leu19=)	PROK2	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1344741	NM_001126128.2(PROK2):c.181A>G (p.Met61Val)	PROK2 (M61V)	Single nucleotide variant (missense variant)	Amenorrhea	GUncertain significance

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