ClinVar (all) for Orgtrack (Select 507795) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 984445	NM_006236.3(POU3F3):c.1018_1019delinsTT (p.Gln340Leu)	POU3F3 (Q340L)	Indel (missense variant)	Snijders blok-fisher syndrome	GLikely pathogenic
Select item 983495	NM_014168.4(METTL5):c.362A>G (p.Asp121Gly)	METTL5 (D121G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity