List of variants in gene IL17RA reported as likely benign for not provided

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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_014339.7(IL17RA):c.1819G>A (p.Glu607Lys)	rs28376631	0.00845
NM_014339.7(IL17RA):c.1530C>T (p.Asp510=)	rs148319877	0.00227
NM_014339.7(IL17RA):c.1689C>T (p.Gly563=)	rs146292661	0.00185
NM_014339.7(IL17RA):c.833G>A (p.Arg278His)	rs141467790	0.00070
NM_014339.7(IL17RA):c.427C>T (p.Arg143Cys)	rs145378071	0.00046
NM_014339.7(IL17RA):c.1088-10G>C	rs941054999	0.00006
NM_014339.7(IL17RA):c.327C>T (p.Leu109=)	rs202060976	0.00005
NM_014339.7(IL17RA):c.932-8C>T	rs769648701	0.00003
NM_014339.7(IL17RA):c.2064C>T (p.Asp688=)	rs184656733	0.00001
NM_014339.7(IL17RA):c.634C>T (p.Leu212=)	rs1046787585	0.00001
NM_014339.7(IL17RA):c.2437GAAGAGGAG[1] (p.Glu816_Glu818del)	rs551742239
NM_014339.7(IL17RA):c.243C>T (p.His81=)	rs1601340999

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