ClinVar for MedGen (Select 1618089) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2691783	NM_001163560.3(MEIOB):c.528+3A>C	MEIOB	Single nucleotide variant (intron variant)	Spermatogenic failure 22	GPathogenic
Select item 2691781	NM_001163560.3(MEIOB):c.1072_1073del (p.Met358fs)	FAHD1, MEIOB (M358fs)	Deletion (frameshift variant +1 more)	Spermatogenic failure 22 +1 more	GPathogenic
Select item 2691780	NM_001163560.3(MEIOB):c.683-1G>A	MEIOB	Single nucleotide variant (splice acceptor variant)	Premature ovarian failure 23 +1 more	GPathogenic
Select item 2691778	NM_001163560.3(MEIOB):c.976G>A (p.Ala326Thr)	MEIOB (A326T)	Single nucleotide variant (missense variant)	Spermatogenic failure 22	GPathogenic
Select item 2045761	NM_001163560.3(MEIOB):c.814C>T (p.Arg272Ter)	MEIOB (R272*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 440759	NM_001163560.3(MEIOB):c.191A>T (p.Asn64Ile)	MEIOB (N64I)	Single nucleotide variant (missense variant)	Spermatogenic failure 22	GPathogenic

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