ClinVar for MedGen (Select 1858807) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3237151	NM_001040274.3(SYCP2L):c.999A>G (p.Ile333Met)	SYCP2L (I333M)	Single nucleotide variant (missense variant)	Premature ovarian failure 24	GPathogenic
Select item 3237150	NM_001040274.3(SYCP2L):c.154_155del (p.Ser52fs)	SYCP2L (S52fs)	Microsatellite (frameshift variant)	Premature ovarian failure 24	GPathogenic