List of variants in gene combination IFNAR2-IL10RB, IL10RB reported as benign 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000628.5(IL10RB):c.*85A>G	rs3171425	0.52896
NM_000628.5(IL10RB):c.*719G>A	rs1058867	0.52783
NM_000628.5(IL10RB):c.139A>G (p.Lys47Glu)	rs2834167	0.24240
NM_000628.5(IL10RB):c.*314G>A	rs8178562	0.14945
NM_000628.5(IL10RB):c.*135G>A	rs8178561	0.08321
NM_000628.5(IL10RB):c.173+19T>C	rs148215894	0.00269
NM_000628.5(IL10RB):c.465T>C (p.Asn155=)	rs138883237	0.00121
NM_000628.5(IL10RB):c.646+19C>A	rs75303005	0.00065
NM_000628.5(IL10RB):c.174-14T>G	rs200472684	0.00046
NM_000628.5(IL10RB):c.645C>T (p.Asp215=)	rs148468217	0.00019
NM_000628.5(IL10RB):c.131C>T (p.Ala44Val)	rs182073431	0.00014
NM_000628.5(IL10RB):c.483C>T (p.Asn161=)	rs61735776	0.00014
NM_000628.5(IL10RB):c.*334G>A	rs377255448	0.00010
NM_000628.5(IL10RB):c.615_616del	rs5843596
NM_000628.5(IL10RB):c.647-7del	rs2123592201

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