NUTM2B-AS1[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3026352	NC_000010.11:g.79723614G>A	NUTM2B-AS1	Single nucleotide variant	not provided	GBenign
Select item 2640645	NC_000010.11:g.79812006A>G	NUTM2B-AS1	Single nucleotide variant	not provided	GLikely benign
Select item 3026454	NC_000010.11:g.79812193T>C	NUTM2B-AS1	Single nucleotide variant	not provided	GUncertain significance
Select item 692219	NR_120611.1:n.192CCG[(35_?)]	NUTM2B-AS1	Microsatellite	Oculopharyngeal myopathy with leukoencephalopathy 1	GPathogenic

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