List of variants in gene PTPN11 reported as benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.14+25G>C	rs7972574	0.05545
NM_002834.5(PTPN11):c.854-21C>T	rs41279090	0.05308
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.525+12G>C	rs41304351	0.01035
NM_002834.5(PTPN11):c.854-30T>C	rs144391508	0.00909
NM_002834.5(PTPN11):c.854-32A>C	rs187389813	0.00867
NM_002834.5(PTPN11):c.1448-38G>C	rs186280715	0.00060
NM_002834.5(PTPN11):c.925A>G (p.Ile309Val)	rs201787206	0.00026
NM_002834.5(PTPN11):c.879C>T (p.His293=)	rs117730996	0.00003
NM_002834.5(PTPN11):c.1650G>A (p.Ala550=)	rs374896287	0.00001
NM_002834.5(PTPN11):c.951G>A (p.Lys317=)	rs576405446	0.00001
NM_002834.5(PTPN11):c.1052G>A (p.Arg351Gln)	rs397507534

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