List of variants in gene IL17RA reported as benign for not specified

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_014339.7(IL17RA):c.932-10C>T	rs2241046	0.81871
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.1458C>T (p.Ile486=)	rs879575	0.20567
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.1819G>A (p.Glu607Lys)	rs28376631	0.00845
NM_014339.7(IL17RA):c.833G>A (p.Arg278His)	rs141467790	0.00070
NM_014339.7(IL17RA):c.1088-45T>G
NM_014339.7(IL17RA):c.138+110T>A
NM_014339.7(IL17RA):c.138+87G>T
NM_014339.7(IL17RA):c.551-110C>T
NM_014339.7(IL17RA):c.551-98C>T
NM_014339.7(IL17RA):c.943+103G>A
NM_014339.7(IL17RA):c.943+122G>C
NM_014339.7(IL17RA):c.943+122_943+123insT
NM_014339.7(IL17RA):c.943+91C>G
NM_014339.7(IL17RA):c.944-112G>A

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