List of variants in gene combination IL17RA, LOC130066894 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014339.7(IL17RA):c.30T>A (p.Ala10=)	rs577217331	0.00204
NM_014339.7(IL17RA):c.-23C>A	rs537206064	0.00027
NM_014339.7(IL17RA):c.-27C>G	rs886057199	0.00010
NM_014339.7(IL17RA):c.-39C>T	rs775719038	0.00006
NM_014339.7(IL17RA):c.8C>T (p.Ala3Val)	rs567320041	0.00006
NM_014339.7(IL17RA):c.26C>T (p.Ser9Phe)	rs752407403	0.00003
NM_014339.7(IL17RA):c.36G>T (p.Pro12=)	rs886057200	0.00001
NM_014339.7(IL17RA):c.-42G>A	rs551693587
NM_014339.7(IL17RA):c.13C>T (p.Arg5Cys)	rs1351337413
NM_014339.7(IL17RA):c.17G>A (p.Ser6Asn)
NM_014339.7(IL17RA):c.23C>T (p.Pro8Leu)	rs2123786576
NM_014339.7(IL17RA):c.41C>G (p.Pro14Arg)
NM_014339.7(IL17RA):c.52CTGCTCCTG[1] (p.Leu21_Leu23del)	rs751990928

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