ClinVar Miner

List of variants reported as benign for Candidiasis, familial, 9

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 40
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_153460.4(IL17RC):c.920A>G (p.Gln307Arg) rs279549 0.99558
NM_153460.4(IL17RC):c.2133C>G (p.Gly711=) rs183956 0.98560
NM_153460.4(IL17RC):c.466-18T>C rs783494 0.54385
NM_153460.4(IL17RC):c.332C>T (p.Ser111Leu) rs708567 0.51321
NM_153460.4(IL17RC):c.1047C>T (p.Asn349=) rs279548 0.22119
NM_153460.4(IL17RC):c.234C>T (p.Thr78=) rs4686383 0.14537
NM_153460.4(IL17RC):c.877+7C>T rs11917994 0.10691
NM_153460.4(IL17RC):c.119G>A (p.Arg40His) rs75324888 0.03978
NM_153460.4(IL17RC):c.1010C>T (p.Pro337Leu) rs115419420 0.03060
NM_153460.4(IL17RC):c.762+9T>A rs115949142 0.02617
NM_153460.4(IL17RC):c.34C>T (p.Leu12=) rs7643547 0.02548
NM_153460.4(IL17RC):c.640G>A (p.Val214Met) rs75692599 0.01226
NM_153460.4(IL17RC):c.970G>A (p.Ala324Thr) rs115461448 0.01170
NM_153460.4(IL17RC):c.622+8C>T rs9864177 0.00908
NM_153460.4(IL17RC):c.1522+1G>C rs148575246 0.00763
NM_153460.4(IL17RC):c.952G>A (p.Ala318Thr) rs145516404 0.00366
NM_153460.4(IL17RC):c.774G>C (p.Gln258His) rs115505677 0.00303
NM_153460.4(IL17RC):c.153G>A (p.Gly51=) rs148170215 0.00301
NM_153460.4(IL17RC):c.591C>T (p.Leu197=) rs139727834 0.00223
NM_153460.4(IL17RC):c.951C>T (p.Asp317=) rs151110374 0.00218
NM_153460.4(IL17RC):c.878-16T>C rs200668081 0.00200
NM_153460.4(IL17RC):c.2025G>A (p.Gly675=) rs189013166 0.00194
NM_153460.4(IL17RC):c.186G>A (p.Ala62=) rs114515915 0.00172
NM_153460.4(IL17RC):c.823-4C>T rs200220568 0.00137
NM_153460.4(IL17RC):c.1680G>A (p.Val560=) rs144732629 0.00109
NM_153460.4(IL17RC):c.1362G>A (p.Ala454=) rs147254895 0.00059
NM_153460.4(IL17RC):c.105+24C>T rs192927730 0.00042
NM_153460.4(IL17RC):c.105+62G>A rs75116348 0.00027
NM_153460.4(IL17RC):c.12C>G (p.Pro4=) rs144276462 0.00024
NM_153460.4(IL17RC):c.1660C>G (p.Leu554Val) rs200293928 0.00024
NM_153460.4(IL17RC):c.957G>A (p.Pro319=) rs200216570 0.00022
NM_153460.4(IL17RC):c.1167G>T (p.Gly389=) rs192723244 0.00019
NM_153460.4(IL17RC):c.1279-18C>T rs753688804 0.00006
NM_153460.4(IL17RC):c.763-16T>G rs199867449 0.00006
NM_153460.4(IL17RC):c.105+123_105+124insCTTTCTGGT rs375878052
NM_153460.4(IL17RC):c.106-138_106-127del rs535660449
NM_153460.4(IL17RC):c.1695G>A (p.Ala565=) rs76999397
NM_153460.4(IL17RC):c.1812C>G (p.Gly604=) rs181990653
NM_153460.4(IL17RC):c.622+115ATTC[5] rs34198416
NM_153460.4(IL17RC):c.877+11C>T rs200861273

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.