List of variants in gene IFNAR1 reported as benign for not provided

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000629.3(IFNAR1):c.502G>C (p.Val168Leu)	rs2257167	0.15608
NM_000629.3(IFNAR1):c.1076C>T (p.Thr359Met)	rs17875834	0.05172
NM_000629.3(IFNAR1):c.213T>C (p.Asp71=)	rs9981753	0.01889
NM_000629.3(IFNAR1):c.1371G>A (p.Ala457=)	rs80214730	0.00570
NM_000629.3(IFNAR1):c.867C>A (p.Thr289=)	rs72552386	0.00300
NM_000629.3(IFNAR1):c.728A>C (p.Asn243Thr)	rs150050372	0.00181
NM_000629.3(IFNAR1):c.624G>A (p.Thr208=)	rs144040431	0.00177
NM_000629.3(IFNAR1):c.189C>T (p.Phe63=)	rs61735334	0.00167
NM_000629.3(IFNAR1):c.201-22_201-19del	rs549440507	0.00123
NM_000629.3(IFNAR1):c.377-11T>C	rs202161321	0.00083
NM_000629.3(IFNAR1):c.916C>T (p.Arg306Cys)	rs201281365	0.00044
NM_000629.3(IFNAR1):c.504T>C (p.Val168=)	rs200831107	0.00016
NM_000629.3(IFNAR1):c.1458A>G (p.Pro486=)	rs770206974	0.00005
NM_000629.3(IFNAR1):c.1440+24dup
NM_000629.3(IFNAR1):c.1587C>T (p.Ser529=)	rs555927601
NM_000629.3(IFNAR1):c.201-10dup	rs747996862

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