List of variants reported as uncertain significance for MHC class I deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001290043.2(TAP2):c.1776G>A (p.Met592Ile)	rs147150415	0.00073
NM_001290043.2(TAP2):c.703C>T (p.Arg235Cys)	rs145890763	0.00023
NM_001290043.2(TAP2):c.1087C>T (p.Arg363Trp)	rs573005983	0.00009
NM_003190.5(TAPBP):c.312del (p.Lys104fs)	rs771157811

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