List of variants reported as likely benign for MHC class I deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000593.6(TAP1):c.997A>G (p.Ile333Val)	rs1057141	0.20047
NM_000593.6(TAP1):c.1910A>G (p.Asp637Gly)	rs1135216	0.17502
NM_001290043.2(TAP2):c.1120G>A (p.Ala374Thr)	rs111303994	0.01475
NM_000593.6(TAP1):c.1976G>A (p.Arg659Gln)	rs121917702	0.00096
NM_000593.6(TAP1):c.1927C>T (p.Leu643=)	rs41559815	0.00037
NM_000593.6(TAP1):c.437C>T (p.Ala146Val)	rs144830209	0.00010
NM_001290043.2(TAP2):c.139G>C (p.Gly47Arg)	rs370260585	0.00001
NM_003190.5(TAPBP):c.174_175delinsTT (p.Asp59Tyr)	rs1554279472

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