Related gene-specific medical variations for Gene (Select 9) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 872865	NM_000662.8(NAT1):c.*215=	NAT1	Variation (no sequence alteration)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 870505	NM_000662.8(NAT1):c.*222=	NAT1	Variation (no sequence alteration)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 815107	GRCh37/hg19 8p22(chr8:18057894-18137250)x1	NAT1	Copy number loss	not provided	GLikely benign
Select item 563437	GRCh37/hg19 8p22(chr8:17969434-18071907)x1	NAT1	Copy number loss	not provided	GLikely benign

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