List of variants in gene IL17RA reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 49

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HGVS	dbSNP	gnomAD frequency
NM_014339.7(IL17RA):c.*5678G>C	rs1654	0.83681
NM_014339.7(IL17RA):c.*2975G>A	rs887796	0.83416
NM_014339.7(IL17RA):c.932-10C>T	rs2241046	0.81871
NM_014339.7(IL17RA):c.*5468T>C	rs4819962	0.72667
NM_014339.7(IL17RA):c.*379G>A	rs2895332	0.72095
NM_014339.7(IL17RA):c.*987G>A	rs882644	0.62420
NM_014339.7(IL17RA):c.*434C>T	rs3179921	0.60485
NM_014339.7(IL17RA):c.*4176T>C	rs738035	0.55900
NM_014339.7(IL17RA):c.*4360T>G	rs5992628	0.55891
NM_014339.7(IL17RA):c.*4205G>A	rs738034	0.55857
NM_014339.7(IL17RA):c.*34T>C	rs1468488	0.32014
NM_014339.7(IL17RA):c.1100C>T (p.Ala367Val)	rs879577	0.29184
NM_014339.7(IL17RA):c.2160C>T (p.Pro720=)	rs4819555	0.25992
NM_014339.7(IL17RA):c.*5519T>C	rs1047929	0.24184
NM_014339.7(IL17RA):c.*3762G>A	rs9606617	0.20762
NM_014339.7(IL17RA):c.1458C>T (p.Ile486=)	rs879575	0.20567
NM_014339.7(IL17RA):c.*5219G>C	rs3827279	0.17336
NM_014339.7(IL17RA):c.*5205C>A	rs3827278	0.17269
NM_014339.7(IL17RA):c.*5612A>G	rs1656	0.17169
NM_014339.7(IL17RA):c.1137G>A (p.Lys379=)	rs879576	0.15008
NM_014339.7(IL17RA):c.2071G>A (p.Ala691Thr)	rs41323645	0.13701
NM_014339.7(IL17RA):c.*4062T>A	rs12484781	0.07666
NM_014339.7(IL17RA):c.*3219A>G	rs5746995	0.07290
NM_014339.7(IL17RA):c.*249A>C	rs5994164	0.02803
NM_014339.7(IL17RA):c.2295G>A (p.Gln765=)	rs41482444	0.02725
NM_014339.7(IL17RA):c.*3060A>G	rs12157837	0.02397
NM_014339.7(IL17RA):c.1685C>A (p.Pro562Gln)	rs12484684	0.02190
NM_014339.7(IL17RA):c.1188G>A (p.Leu396=)	rs2229151	0.02175
NM_014339.7(IL17RA):c.*5256C>T	rs1003944	0.01864
NM_014339.7(IL17RA):c.*5270C>T	rs1003943	0.01714
NM_014339.7(IL17RA):c.*5659G>A	rs7289055	0.01147
NM_014339.7(IL17RA):c.*5036C>T	rs1003945	0.01136
NM_014339.7(IL17RA):c.1819G>A (p.Glu607Lys)	rs28376631	0.00845
NM_014339.7(IL17RA):c.*238G>C	rs143922111	0.00671
NM_014339.7(IL17RA):c.*2112C>T	rs12159073	0.00663
NM_014339.7(IL17RA):c.*1379A>T	rs5992627	0.00655
NM_014339.7(IL17RA):c.*2111C>T	rs114684847	0.00510
NM_014339.7(IL17RA):c.1747G>C (p.Asp583His)	rs41432148	0.00389
NM_014339.7(IL17RA):c.833G>A (p.Arg278His)	rs141467790	0.00070
NM_014339.7(IL17RA):c.2389A>G (p.Ile797Val)	rs74827998	0.00018
NM_014339.7(IL17RA):c.*2163G>C	rs543545127	0.00013
NM_014339.7(IL17RA):c.*3976G>A	rs576803215	0.00009
NM_014339.7(IL17RA):c.*2066G>C	rs375958748	0.00005
NM_014339.7(IL17RA):c.*3624G>A	rs563135481	0.00005
NM_014339.7(IL17RA):c.*3265del	rs398040433
NM_014339.7(IL17RA):c.*5779dup	rs11389817
NM_014339.7(IL17RA):c.*696del	rs35219112
NM_014339.7(IL17RA):c.*803G>A	rs12158721
NM_014339.7(IL17RA):c.138+12C>T	rs534287611

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