ClinVar for OMIM (Select 617673) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 2691779	NM_001163560.3(MEIOB):c.1218G>A (p.Thr406=)	FAHD1, MEIOB	Single nucleotide variant (synonymous variant +1 more)	Premature ovarian failure 23	GPathogenic
Select item 2045761	NM_001163560.3(MEIOB):c.814C>T (p.Arg272Ter)	MEIOB (R272*)	Single nucleotide variant (nonsense)	not provided	GPathogenic

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