List of variants in gene combination LOC130009573, RFXAP reported as uncertain significance for immune system disorder

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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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000538.4(RFXAP):c.-101T>G	rs566055344	0.00037
NM_000538.4(RFXAP):c.-82G>C	rs1049387935	0.00036
NM_000538.4(RFXAP):c.77C>G (p.Pro26Arg)	rs763162669	0.00019
NM_000538.4(RFXAP):c.14G>T (p.Gly5Val)	rs571468892	0.00005
NM_000538.4(RFXAP):c.148C>A (p.Gln50Lys)	rs1267956141	0.00004
NM_000538.4(RFXAP):c.-116C>G	rs886050141	0.00003
NM_000538.4(RFXAP):c.118G>T (p.Ala40Ser)	rs1320172546	0.00003
NM_000538.4(RFXAP):c.55C>T (p.Pro19Ser)	rs1483760429	0.00003
NM_000538.3(RFXAP):c.-144G>A	rs886050140	0.00001
NM_000538.4(RFXAP):c.-131C>T	rs1021353605	0.00001
NM_000538.4(RFXAP):c.15T>C (p.Gly5=)	rs772887500	0.00001
NM_000538.4(RFXAP):c.44C>T (p.Ala15Val)	rs1344939848	0.00001
NM_000538.4(RFXAP):c.59A>G (p.His20Arg)	rs775615242	0.00001
NM_000538.3(RFXAP):c.-142T>C	rs2057951998
NM_000538.4(RFXAP):c.-105C>A	rs527311083
NM_000538.4(RFXAP):c.101C>G (p.Pro34Arg)	rs2057953877
NM_000538.4(RFXAP):c.108_125del (p.Val37_Ser42del)	rs1266956441
NM_000538.4(RFXAP):c.115G>C (p.Ala39Pro)	rs1024812180
NM_000538.4(RFXAP):c.150A>T (p.Gln50His)	rs761195790
NM_000538.4(RFXAP):c.152C>T (p.Pro51Leu)	rs2057954189
NM_000538.4(RFXAP):c.20C>T (p.Ala7Val)
NM_000538.4(RFXAP):c.29C>T (p.Ala10Val)
NM_000538.4(RFXAP):c.2T>C (p.Met1Thr)	rs2057953200
NM_000538.4(RFXAP):c.51C>T (p.Gly17=)	rs2138212292
NM_000538.4(RFXAP):c.52G>T (p.Val18Leu)	rs1232670161
NM_000538.4(RFXAP):c.58C>T (p.His20Tyr)	rs1555302467

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