List of variants in gene combination NR2C2AP, RFXANK reported as likely benign for MHC class II deficiency

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_003721.4(RFXANK):c.*9T>C	rs73922832	0.03001
NM_003721.4(RFXANK):c.751C>G (p.Gln251Glu)	rs1802498	0.00545
NM_003721.4(RFXANK):c.713-20T>C	rs778907929	0.00009
NM_003721.4(RFXANK):c.775C>T (p.Pro259Ser)	rs199868077	0.00009
NM_003721.4(RFXANK):c.741C>G (p.Leu247=)	rs768433483	0.00003
NM_003721.4(RFXANK):c.713-6T>C	rs757150693	0.00001
NM_003721.4(RFXANK):c.713-8C>G	rs752799290	0.00001
NM_003721.4(RFXANK):c.713-5C>A
NM_003721.4(RFXANK):c.713-7A>G
NM_003721.4(RFXANK):c.759C>T (p.Asn253=)
NM_003721.4(RFXANK):c.762G>T (p.Leu254=)

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