List of variants in gene combination IL21R, LOC130058712 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_181078.3(IL21R):c.1033G>A (p.Gly345Ser)	rs56148525	0.00271
NM_181078.3(IL21R):c.995C>T (p.Thr332Met)	rs761814669	0.00007
NM_181078.3(IL21R):c.1034G>A (p.Gly345Asp)	rs759242116	0.00004
NM_181078.3(IL21R):c.1021G>A (p.Val341Met)	rs1017631687	0.00001
NM_181078.3(IL21R):c.980A>C (p.Lys327Thr)	rs747283184	0.00001
NM_181078.3(IL21R):c.1001T>C (p.Leu334Pro)
NM_181078.3(IL21R):c.1003C>A (p.Gln335Lys)	rs954730051
NM_181078.3(IL21R):c.1013C>T (p.Ala338Val)	rs2087529653
NM_181078.3(IL21R):c.1028C>G (p.Ser343Cys)	rs2141318837
NM_181078.3(IL21R):c.1030G>C (p.Asp344His)
NM_181078.3(IL21R):c.983G>A (p.Arg328Lys)
NM_181078.3(IL21R):c.985C>G (p.Leu329Val)

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