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

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 756682	NM_001002292.4(WLS):c.1554del (p.Phe518fs)	GNG12-AS1, WLS (F518fs)	Deletion (non-coding transcript variant +1 more)	WLS-related disorder +1 more	GBenign/Likely benign
Select item 3029388	NM_024911.7(WLS):c.1363-3279C>A	GNG12-AS1, WLS	Single nucleotide variant (intron variant)	WLS-related disorder	GUncertain significance
Select item 3053025	NM_024911.7(WLS):c.505-10C>A	GNG12-AS1, WLS	Single nucleotide variant (intron variant)	WLS-related disorder	GLikely benign
Select item 3030845	NM_024911.7(WLS):c.138_169dup (p.His57delinsArgArgTer)	GNG12-AS1, WLS	Duplication (nonsense +1 more)	WLS-related disorder	GUncertain significance

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