ClinVar Miner

List of variants in gene CLN6 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_017882.3(CLN6):c.*141_*142GT[13] rs3837692
NM_017882.3(CLN6):c.*393G>A
NM_017882.3(CLN6):c.*646C>G rs144976448
NM_017882.3(CLN6):c.*655C>T
NM_017882.3(CLN6):c.*75G>C
NM_017882.3(CLN6):c.*934G>T rs114551417
NM_017882.3(CLN6):c.42C>A (p.Gly14=) rs373776911
NM_017882.3(CLN6):c.5A>G (p.Glu2Gly) rs3743088
NM_017882.3(CLN6):c.64G>T (p.Ala22Ser) rs527373013
NM_017882.3(CLN6):c.769A>G (p.Ser257Gly) rs151295143

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.