ClinVar (all) for Orgtrack (Select 508985) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2571587	NM_020796.5(SEMA6A):c.1268T>C (p.Ile423Thr)	SEMA6A (I423T)	Single nucleotide variant (missense variant)	Delayed puberty, self-limited	GLikely pathogenic
Select item 2443311	NM_181303.2(NLGN3):c.366G>A (p.Trp122Ter)	NLGN3 (W122* +1 more)	Single nucleotide variant (nonsense)	Hypogonadotropic hypogonadism	GPathogenic