List of variants in gene combination LOC130009574, RFXAP reported as benign for immune system disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000538.4(RFXAP):c.410T>C (p.Met137Thr)	rs193240312	0.01125
NM_000538.4(RFXAP):c.430G>A (p.Glu144Lys)	rs201754085	0.00009

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