List of variants in gene PTPN11 reported as likely benign for bone disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.*1006del	rs146940557	0.05739
NM_002834.5(PTPN11):c.526-17T>C	rs375184329	0.00096
NM_002834.5(PTPN11):c.1658C>T (p.Thr553Met)	rs148176616	0.00048
NM_002834.5(PTPN11):c.1379+20C>T	rs184743462	0.00047
NM_002834.5(PTPN11):c.643-6dup	rs758889732	0.00030
NM_002834.5(PTPN11):c.1746C>T (p.Asn582=)	rs397516800	0.00013
NM_002834.5(PTPN11):c.1224+15G>A	rs373271861	0.00011
NM_002834.5(PTPN11):c.558G>T (p.Arg186=)	rs200920312	0.00011
NM_002834.5(PTPN11):c.1449T>G (p.Gly483=)	rs143238917	0.00009
NM_002834.5(PTPN11):c.1678C>T (p.Leu560Phe)	rs397516797	0.00007
NM_002834.5(PTPN11):c.392A>G (p.Lys131Arg)	rs397516805	0.00006
NM_002834.5(PTPN11):c.616T>C (p.Leu206=)	rs78376169	0.00006
NM_002834.5(PTPN11):c.14+11C>A	rs1486505121	0.00004
NM_002834.5(PTPN11):c.327T>G (p.Ser109=)	rs1039250039	0.00002
NM_002834.5(PTPN11):c.1011G>A (p.Thr337=)	rs371951288	0.00001
NM_002834.5(PTPN11):c.1047C>T (p.Asn349=)	rs1222504763	0.00001
NM_002834.5(PTPN11):c.1131A>C (p.Leu377=)	rs370059077	0.00001
NM_002834.5(PTPN11):c.1233G>A (p.Thr411=)	rs1325353647	0.00001
NM_002834.5(PTPN11):c.1650G>A (p.Ala550=)	rs374896287	0.00001
NM_002834.5(PTPN11):c.874C>T (p.Leu292=)	rs930267460	0.00001
NM_002834.5(PTPN11):c.*1157ATG[14]	rs80269561
NM_002834.5(PTPN11):c.519C>G (p.Arg173=)	rs767425313
NM_002834.5(PTPN11):c.643-61_643-38del	rs1592831434

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