"MIAT-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2691795	NR_003491.3(MIAT):n.1132G>A	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3057049	NR_003491.3(MIAT):n.1428G>A	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 2691796	NR_003491.3(MIAT):n.1505G>A	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3035661	NR_003491.3(MIAT):n.1590G>T	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3056260	NR_003491.3(MIAT):n.3477G>C	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3037110	NR_003491.3(MIAT):n.3588G>C	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GLikely benign
Select item 3055781	NR_003491.3(MIAT):n.3777dup	MIAT	Duplication (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3036351	NR_003491.3(MIAT):n.4308_4311dup	MIAT	Duplication (non-coding transcript variant)	MIAT-related disorder	GLikely benign
Select item 3060877	NR_003491.3(MIAT):n.4966G>T	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3059963	NR_003491.3(MIAT):n.5534C>T	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3056598	NR_003491.3(MIAT):n.5794A>T	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3046181	NR_003491.3(MIAT):n.5895C>T	MIAT	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign
Select item 3057060	NR_003491.3(MIAT):n.6996G>T	MIAT, MIATNB	Single nucleotide variant (non-coding transcript variant)	MIAT-related disorder	GBenign