List of variants in gene RFXAP reported as likely pathogenic for MHC class II deficiency 4

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_000538.4(RFXAP):c.259del (p.Glu87fs)
NM_000538.4(RFXAP):c.323T>A (p.Leu108Ter)	rs754240018
NM_000538.4(RFXAP):c.696_700del (p.Asn232fs)

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