List of variants in gene combination IL17RA, LOC126863094 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014339.7(IL17RA):c.1087G>A (p.Asp363Asn)	rs149771513	0.00051
NM_014339.7(IL17RA):c.1086C>T (p.Thr362=)	rs139716919	0.00022
NM_014339.7(IL17RA):c.1046G>C (p.Gly349Ala)	rs143897670	0.00015
NM_014339.7(IL17RA):c.1085C>T (p.Thr362Ile)	rs371565499	0.00010
NM_014339.7(IL17RA):c.1067G>A (p.Ser356Asn)	rs777845932	0.00001
NM_014339.7(IL17RA):c.1081T>C (p.Tyr361His)	rs34545718	0.00001
NM_014339.7(IL17RA):c.1086C>A (p.Thr362=)	rs139716919

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