ClinVar (all) for Orgtrack (Select 508404) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 975953	NM_005321.3(H1-4):c.365dup (p.Ala123fs)	H1-4 (A123fs)	Duplication (frameshift variant)	not provided +1 more	GPathogenic
Select item 428605	NM_005321.3(H1-4):c.430dup (p.Ala144fs)	H1-4 (A144fs)	Duplication (frameshift variant)	Inborn genetic diseases +2 more	GPathogenic/Likely pathogenic