"PreventionGenetics, part of Exact Sciences"[submitter] AND "ST7"[gene - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055413	NM_001369598.1(ST7):c.1078+7T>C	ST7	Single nucleotide variant (intron variant)	ST7-related disorder	GBenign
Select item 3039795	NM_001369598.1(ST7):c.1395G>A (p.Thr465=)	ST7, ST7-OT3	Single nucleotide variant (synonymous variant +2 more)	ST7-related disorder	GLikely benign
Select item 3057920	NM_001369598.1(ST7):c.1406-8G>A	ST7	Single nucleotide variant (intron variant)	ST7-related disorder	GLikely benign
Select item 743510	NM_001369598.1(ST7):c.1638+917G>T	ST7	Single nucleotide variant (stop lost +1 more)	not provided +1 more	GLikely benign
Select item 3040627	NM_001369598.1(ST7):c.1639-3C>A	ST7	Single nucleotide variant (intron variant)	ST7-related disorder	GLikely benign

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