ClinVar (all) for Orgtrack (Select 507268) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 810691	NM_014009.4(FOXP3):c.691C>A (p.Gln231Lys)	FOXP3 (Q196K +1 more)	Single nucleotide variant (missense variant)	Non-obstructive azoospermia	GPathogenic
Select item 712945	NM_014009.4(FOXP3):c.155G>T (p.Gly52Val)	FOXP3 (G52V)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign