ClinVar (all) for Orgtrack (Select 500298) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 37115	NM_144605.5(SEPTIN12):c.589G>A (p.Asp197Asn)	SEPTIN12 (D197N +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 10	Grisk factor
Select item 37114	NM_144605.5(SEPTIN12):c.266C>T (p.Thr89Met)	SEPTIN12 (T89M)	Single nucleotide variant (missense variant)	Spermatogenic failure 10	Grisk factor