"PreventionGenetics, part of Exact Sciences"[submitter] AND "MCIDAS"[g - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 525544	NM_001190787.3(MCIDAS):c.1050C>G (p.Thr350=)	MCIDAS	Single nucleotide variant (synonymous variant)	MCIDAS-related disorder +1 more	GLikely benign
Select item 238623	NM_001190787.3(MCIDAS):c.856G>A (p.Glu286Lys)	MCIDAS (E286K)	Single nucleotide variant (missense variant)	MCIDAS-related disorder +1 more	GBenign/Likely benign
Select item 2636931	NM_001190787.3(MCIDAS):c.229A>G (p.Ile77Val)	MCIDAS (I77V)	Single nucleotide variant (missense variant)	MCIDAS-related disorder	GUncertain significance
Select item 454527	NM_001190787.3(MCIDAS):c.218-13_218-6dup	MCIDAS	Duplication (intron variant)	MCIDAS-related disorder +2 more	GLikely benign
Select item 525567	NM_001190787.3(MCIDAS):c.93C>G (p.Leu31=)	MCIDAS	Single nucleotide variant (synonymous variant)	MCIDAS-related disorder +1 more	GBenign/Likely benign

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