List of variants in gene combination IL17RA, LOC129391259 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_014339.7(IL17RA):c.958T>C (p.Trp320Arg)	rs140221307	0.00230
NM_014339.7(IL17RA):c.978G>A (p.Thr326=)	rs143239201	0.00060
NM_014339.7(IL17RA):c.1006G>A (p.Val336Ile)	rs138404135	0.00011
NM_014339.7(IL17RA):c.1021G>A (p.Val341Ile)	rs868826492	0.00006
NM_014339.7(IL17RA):c.1045+6C>T	rs763664351	0.00004
NM_014339.7(IL17RA):c.949A>G (p.Met317Val)	rs1208693308	0.00004
NM_014339.7(IL17RA):c.960G>T (p.Trp320Cys)	rs758399114	0.00002
NM_014339.7(IL17RA):c.1045+7G>A	rs572837622	0.00001
NM_014339.7(IL17RA):c.952C>T (p.Pro318Ser)	rs200724343	0.00001
NM_014339.7(IL17RA):c.995T>C (p.Leu332Pro)	rs1414561554	0.00001
NM_014339.7(IL17RA):c.1030A>G (p.Thr344Ala)	rs2061413259
NM_014339.7(IL17RA):c.1038G>C (p.Arg346Ser)	rs2123807952
NM_014339.7(IL17RA):c.944-6C>A	rs2123807788
NM_014339.7(IL17RA):c.996_997delinsCT (p.Val333Leu)	rs2061413124

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