List of variants in gene combination LOC126805858, RFX5 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_001025603.2(RFX5):c.-91G>A	rs555635380	0.00081
NM_001025603.2(RFX5):c.-131-15T>C	rs190371864	0.00019
NM_001025603.2(RFX5):c.-131-8C>A	rs886045284

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