List of variants in gene combination AP4B1, PTPN22 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015967.8(PTPN22):c.147T>C (p.Ala49=)	rs61745743	0.00717
NM_015967.8(PTPN22):c.2075C>G (p.Ser692Cys)	rs183145687	0.00230
NM_015967.8(PTPN22):c.197-4A>G	rs72650669	0.00141
NM_015967.8(PTPN22):c.1514C>G (p.Ser505Cys)	rs570783720	0.00089

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