List of variants in gene PTPN11 reported as benign by Invitae

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_002834.3(PTPN11):c.-273G>A	rs58805176	0.10884
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.332+17T>G	rs115658366	0.00257
NM_002834.5(PTPN11):c.526-17T>C	rs375184329	0.00096
NM_002834.5(PTPN11):c.526-8C>A	rs184804143	0.00064
NM_002834.5(PTPN11):c.1379+20C>T	rs184743462	0.00047
NM_002834.5(PTPN11):c.558G>T (p.Arg186=)	rs200920312	0.00011
NM_002834.5(PTPN11):c.1092+10A>G	rs758723402	0.00001
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.1221A>G (p.Gly407=)	rs532529560
NM_002834.5(PTPN11):c.15-4del	rs1223869705
NM_002834.5(PTPN11):c.1713-14dup

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