List of variants in gene RFXANK reported as benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003721.4(RFXANK):c.213C>T (p.Thr71=)	rs72997200	0.04571
NM_003721.4(RFXANK):c.144G>C (p.Glu48Asp)	rs34282046	0.04400
NM_003721.4(RFXANK):c.712+4A>G	rs73922830	0.03058
NM_003721.4(RFXANK):c.439-13C>T	rs181297102	0.00339
NM_003721.4(RFXANK):c.337+4C>T	rs187331767	0.00316
NM_003721.4(RFXANK):c.188-11C>T	rs201545133	0.00029
NM_003721.4(RFXANK):c.280A>G (p.Ile94Val)
NM_003721.4(RFXANK):c.535C>T (p.Arg179Cys)	rs115964828

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