List of variants in gene PTPN11 reported as benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.1093-9C>A	rs12301915	0.04151
NM_002834.5(PTPN11):c.255C>T (p.His85=)	rs61736914	0.02271
NM_002834.5(PTPN11):c.526-8C>A	rs184804143	0.00062
NM_002834.5(PTPN11):c.643-6dup	rs758889732	0.00030

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