List of variants reported as uncertain significance for immune system disorder by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000271.5(NPC1):c.3550G>A (p.Val1184Met)	rs767795351	0.00011
NM_014009.4(FOXP3):c.361C>T (p.His121Tyr)	rs782640594	0.00007
NM_001199138.2(NLRC4):c.2728G>A (p.Val910Ile)	rs144418059	0.00003
NM_000064.4(C3):c.1125C>A (p.Phe375Leu)
NM_000271.5(NPC1):c.1408G>C (p.Ala470Pro)
NM_000271.5(NPC1):c.2509A>G (p.Ile837Val)	rs756239485
NM_001291746.2(REL):c.659T>C (p.Phe220Ser)
NM_006767.4(LZTR1):c.370G>A (p.Val124Ile)
NM_006939.4(SOS2):c.3303T>G (p.Ser1101Arg)	rs1317870927

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