Related gene-specific medical variations for Gene (Select 4808) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1326289	NM_005599.3(NHLH2):c.25G>T (p.Ala9Ser)	NHLH2 (A9S)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism	GUncertain significance
Select item 1326269	NM_005599.3(NHLH2):c.91G>A (p.Val31Met)	NHLH2 (V31M)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism	GUncertain significance
Select item 1326268	NM_005599.3(NHLH2):c.26C>T (p.Ala9Val)	NHLH2 (A9V)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism	GUncertain significance

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