List of variants in gene combination AP4B1, PTPN22 reported as uncertain significance for autoimmune disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015967.8(PTPN22):c.1894+2T>C
NM_015967.8(PTPN22):c.841del (p.Leu281fs)
NM_015967.8(PTPN22):c.91C>G (p.Leu31Val)

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