ClinVar for OMIM (Select 615413) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 65392	NM_199461.2(NANOS1):c.[737G>A;826_827delinsTA]	LOC130004822, NANOS1 (R276Y +1 more)	Indel (missense variant)	Spermatogenic failure 12	GPathogenic
Select item 65391	NM_199461.4(NANOS1):c.502GCC[5] (p.Ala173del)	NANOS1 (A173del)	Microsatellite (inframe_deletion)	Spermatogenic failure 12	GPathogenic
Select item 65390	NM_199461.4(NANOS1):c.231CTC[3] (p.Ser83del)	LOC130004821, NANOS1 (S83del)	Microsatellite (inframe_deletion)	not provided +1 more	GBenign/Likely benign

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