List of variants in gene combination PSMB8, TAP1 reported as benign for MHC class I deficiency

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_000593.6(TAP1):c.2182C>A (p.Gln728Lys)	rs74897484	0.00175
NM_000593.6(TAP1):c.2041-14A>C	rs140017767	0.00145
NM_000593.6(TAP1):c.2041-15G>A	rs538476075	0.00001

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