ClinVar Miner

List of variants reported as likely benign for Candidiasis, familial, 6 by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_052872.4(IL17F):c.360C>T (p.Ser120=) rs536968854 0.00010
NM_052872.4(IL17F):c.243C>G (p.Pro81=) rs769617558 0.00007
NM_052872.4(IL17F):c.255-5T>C rs972404643 0.00006
NM_052872.4(IL17F):c.34-17C>T rs762219876 0.00003
NM_052872.4(IL17F):c.427T>C (p.Leu143=) rs1015495067 0.00003
NM_052872.4(IL17F):c.159T>C (p.Gly53=) rs748990409 0.00001
NM_052872.4(IL17F):c.174C>T (p.Asp58=) rs889879171 0.00001
NM_052872.4(IL17F):c.177T>C (p.Ile59=) rs1433771627 0.00001
NM_052872.4(IL17F):c.273C>T (p.Asn91=) rs775184787 0.00001
NM_052872.4(IL17F):c.345C>T (p.Asp115=) rs137981743 0.00001
NM_052872.4(IL17F):c.387C>T (p.Val129=) rs765197624 0.00001
NM_052872.4(IL17F):c.462C>T (p.Cys154=) rs780312510 0.00001
NM_052872.4(IL17F):c.54G>A (p.Ser18=) rs772321235 0.00001
NM_052872.4(IL17F):c.58T>C (p.Leu20=) rs374833689 0.00001
NM_052872.4(IL17F):c.102C>G (p.Pro34=)
NM_052872.4(IL17F):c.111A>G (p.Gly37=)
NM_052872.4(IL17F):c.114T>C (p.His38=)
NM_052872.4(IL17F):c.144G>A (p.Pro48=)
NM_052872.4(IL17F):c.144G>C (p.Pro48=)
NM_052872.4(IL17F):c.15C>G (p.Thr5=)
NM_052872.4(IL17F):c.180C>A (p.Gly60=) rs2128267796
NM_052872.4(IL17F):c.201C>T (p.Arg67=)
NM_052872.4(IL17F):c.254+5G>C rs571390206
NM_052872.4(IL17F):c.255-7C>T
NM_052872.4(IL17F):c.255-9C>T rs374838092
NM_052872.4(IL17F):c.258C>A (p.Val86=) rs2128267452
NM_052872.4(IL17F):c.270C>T (p.Pro90=)
NM_052872.4(IL17F):c.288A>G (p.Glu96=)
NM_052872.4(IL17F):c.291T>C (p.Val97=) rs2128267440
NM_052872.4(IL17F):c.33+12C>T
NM_052872.4(IL17F):c.34-16G>A
NM_052872.4(IL17F):c.351C>T (p.Ser117=)
NM_052872.4(IL17F):c.375A>G (p.Gln125=)
NM_052872.4(IL17F):c.39G>A (p.Lys13=)
NM_052872.4(IL17F):c.411C>T (p.Cys137=)
NM_052872.4(IL17F):c.413_414del (p.Ser138fs) rs11465552
NM_052872.4(IL17F):c.447T>A (p.Thr149=)
NM_052872.4(IL17F):c.456C>T (p.Cys152=) rs1345707985
NM_052872.4(IL17F):c.459C>T (p.Thr153=)
NM_052872.4(IL17F):c.477C>A (p.Ile159=)
NM_052872.4(IL17F):c.483T>C (p.His161=)
NM_052872.4(IL17F):c.96A>G (p.Lys32=)

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