Variants in gene PTPN11 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.173A>G (p.Asn58Ser)	rs751437780	0.00004
NM_002834.5(PTPN11):c.1282G>A (p.Val428Met)	rs397507536	0.00003
NM_002834.5(PTPN11):c.794G>T (p.Arg265Leu)	rs376607329	0.00003
NM_002834.5(PTPN11):c.1382C>G (p.Ala461Gly)	rs397509344
NM_002834.5(PTPN11):c.1402A>G (p.Thr468Ala)	rs397507537
NM_002834.5(PTPN11):c.155C>T (p.Thr52Ile)	rs397507503
NM_002834.5(PTPN11):c.205G>A (p.Glu69Lys)	rs397507511
NM_002834.5(PTPN11):c.227A>G (p.Glu76Gly)	rs121918465
NM_002834.5(PTPN11):c.329A>G (p.Glu110Gly)	rs397507519
NM_002834.5(PTPN11):c.762ACA[2] (p.Gln257del)	rs397507524
NM_002834.5(PTPN11):c.782T>G (p.Leu261Arg)	rs765642157
NM_002834.5(PTPN11):c.853T>G (p.Phe285Val)	rs397507531

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