List of variants in gene combination IL17RC, LOC129936143 reported as uncertain significance for immune system disorder

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_153460.4(IL17RC):c.1519G>A (p.Gly507Arg)	rs763525201	0.00001
NM_153460.4(IL17RC):c.1487G>A (p.Trp496Ter)	rs760707054
NM_153460.4(IL17RC):c.1490T>C (p.Leu497Pro)
NM_153460.4(IL17RC):c.1493G>A (p.Arg498Lys)
NM_153460.4(IL17RC):c.1509C>G (p.Asp503Glu)
NM_153460.4(IL17RC):c.1514G>A (p.Arg505His)	rs2084894919
NM_153460.4(IL17RC):c.1519G>C (p.Gly507Arg)	rs763525201
NM_153460.4(IL17RC):c.1522+1dup	rs1341716326
NM_153460.4(IL17RC):c.1522+3G>T	rs2084898305

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.