List of variants in gene combination CIITA, LOC130058442 reported as uncertain significance for MHC class II 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_000246.4(CIITA):c.-84C>T	rs45519531	0.00447
NM_000246.4(CIITA):c.-83C>T	rs534663824	0.00015
NM_000246.4(CIITA):c.-82G>A	rs886051635	0.00001

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