List of variants in gene IL17RA reported as likely 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: 39

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HGVS	dbSNP	gnomAD frequency
NM_014339.7(IL17RA):c.2338_2339del	rs57380532	0.13907
NM_014339.7(IL17RA):c.*3913C>T	rs11702918	0.12934
NM_014339.7(IL17RA):c.*3506A>G	rs9605216	0.12423
NM_014339.7(IL17RA):c.*1113C>G	rs882643	0.12223
NM_014339.7(IL17RA):c.*4045G>A	rs11703539	0.11955
NM_014339.7(IL17RA):c.*4956G>A	rs12106586	0.06615
NM_014339.7(IL17RA):c.*3999G>A	rs60065827	0.06106
NM_014339.7(IL17RA):c.*3812T>C	rs56711032	0.06090
NM_014339.7(IL17RA):c.*3938G>A	rs73876646	0.05976
NM_014339.7(IL17RA):c.*5314T>C	rs73876647	0.05311
NM_014339.7(IL17RA):c.*2314A>G	rs56069130	0.05309
NM_014339.7(IL17RA):c.*2175C>A	rs55893323	0.05260
NM_014339.7(IL17RA):c.*4465C>T	rs62623403	0.04390
NM_014339.7(IL17RA):c.*4267A>G	rs11913443	0.03646
NM_014339.7(IL17RA):c.*2721A>G	rs56004960	0.03594
NM_014339.7(IL17RA):c.799_800del	rs143534372	0.02338
NM_014339.7(IL17RA):c.*2427T>C	rs114538254	0.02175
NM_014339.7(IL17RA):c.*2100A>G	rs12160599	0.01517
NM_014339.7(IL17RA):c.551-9G>T	rs17205308	0.00859
NM_014339.7(IL17RA):c.*1686G>A	rs144428545	0.00780
NM_014339.7(IL17RA):c.2490C>T (p.Pro830=)	rs3804060	0.00761
NM_014339.7(IL17RA):c.*5677C>A	rs559845151	0.00452
NM_014339.7(IL17RA):c.*399C>T	rs12157751	0.00374
NM_014339.7(IL17RA):c.1174G>T (p.Val392Leu)	rs146478431	0.00249
NM_014339.7(IL17RA):c.152C>T (p.Thr51Met)	rs143008696	0.00223
NM_014339.7(IL17RA):c.1689C>T (p.Gly563=)	rs146292661	0.00185
NM_014339.7(IL17RA):c.*4197A>G	rs149359202	0.00148
NM_014339.7(IL17RA):c.*4124G>T	rs138712036	0.00113
NM_014339.7(IL17RA):c.*3187T>G	rs536506632	0.00096
NM_014339.7(IL17RA):c.*4004C>T	rs150231194	0.00068
NM_014339.7(IL17RA):c.*2603C>T	rs192250812	0.00031
NM_014339.7(IL17RA):c.*320A>G	rs577387326	0.00014
NM_014339.7(IL17RA):c.2264T>C (p.Leu755Pro)	rs574409116	0.00013
NM_014339.7(IL17RA):c.655G>T (p.Val219Leu)	rs186541010	0.00011
NM_014339.7(IL17RA):c.*1338G>A	rs192058258
NM_014339.7(IL17RA):c.*2344C>T	rs4563337
NM_014339.7(IL17RA):c.*3179dup	rs547906480
NM_014339.7(IL17RA):c.*4003G>T	rs143888540
NM_014339.7(IL17RA):c.942G>A (p.Pro314=)	rs41321447

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