List of variants in gene IL17RC reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_153460.4(IL17RC):c.161T>C (p.Val54Ala)	rs138985119	0.00220
NM_153460.4(IL17RC):c.1768A>G (p.Ser590Gly)	rs141404925	0.00168
NM_153460.4(IL17RC):c.969C>T (p.Pro323=)	rs137952141	0.00118
NM_153460.4(IL17RC):c.1523-33A>C
NM_153460.4(IL17RC):c.1803G>A (p.Gly601=)	rs2125318610
NM_153460.4(IL17RC):c.273C>A (p.Ala91=)	rs1205369392

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