List of variants in gene PTPRF reported as benign for not provided

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002840.5(PTPRF):c.1806C>A (p.Ala602=)	rs3828151	0.41982
NM_002840.5(PTPRF):c.234C>T (p.Phe78=)	rs6684279	0.03172
NM_002840.5(PTPRF):c.3974-9C>T	rs72877532	0.02182
NM_002840.5(PTPRF):c.4977C>T (p.Ala1659=)	rs61734379	0.00291
NM_002840.5(PTPRF):c.1531+9G>A	rs188853413	0.00253
NM_002840.5(PTPRF):c.5136A>C (p.Thr1712=)	rs143019283	0.00243
NM_002840.5(PTPRF):c.4539C>T (p.Ala1513=)	rs141505475	0.00198
NM_002840.5(PTPRF):c.237+5G>A	rs144175107	0.00184
NM_002840.5(PTPRF):c.1668+9C>T	rs141736132	0.00155
NM_002840.5(PTPRF):c.3876G>A (p.Pro1292=)	rs139339462	0.00152
NM_002840.5(PTPRF):c.2526A>G (p.Pro842=)	rs145092417	0.00151
NM_002840.5(PTPRF):c.4821T>C (p.Ala1607=)	rs145219690	0.00086
NM_002840.5(PTPRF):c.1113C>T (p.Thr371=)	rs3748795	0.00076
NM_002840.5(PTPRF):c.2825C>T (p.Ala942Val)	rs144156070	0.00068
NM_002840.5(PTPRF):c.1903C>T (p.Arg635Cys)	rs17849101	0.00042
NM_002840.5(PTPRF):c.663G>A (p.Ala221=)	rs540168118	0.00001
NM_002840.5(PTPRF):c.1668+10G>C	rs201946505

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