List of variants reported as uncertain significance for autoimmune disease by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000383.4(AIRE):c.485C>T (p.Pro162Leu)	rs138949170	0.00009
NM_014009.4(FOXP3):c.967+4A>G	rs1426535368

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