ClinVar Miner

List of variants in gene CLCN7 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001287.6(CLCN7):c.*1389A>C rs710900 0.90699
NM_001287.6(CLCN7):c.*887C>T rs6600146 0.85737
NM_001287.6(CLCN7):c.*886C>T rs1050834 0.85735
NM_001287.6(CLCN7):c.*1626G>C rs8767 0.60777
NM_001287.6(CLCN7):c.1170A>T (p.Ala390=) rs2235579 0.51407
NM_001287.6(CLCN7):c.*735C>T rs2294542 0.51156
NM_001287.6(CLCN7):c.*1332C>T rs941439 0.37181
NM_001287.6(CLCN7):c.660C>T (p.His220=) rs12923538 0.14578
NM_001287.6(CLCN7):c.485-10T>C rs35280276 0.13624
NM_001287.6(CLCN7):c.*627A>G rs10903009 0.12292
NM_001287.6(CLCN7):c.*19A>G rs11860968 0.11981
NM_001287.6(CLCN7):c.1798-8G>A rs35915213 0.10339
NM_001287.6(CLCN7):c.1245T>C (p.Ile415=) rs12926669 0.09695
NM_001287.6(CLCN7):c.1128G>A (p.Pro376=) rs12935737 0.06897
NM_001287.6(CLCN7):c.1614G>A (p.Ala538=) rs117461525 0.06889
NM_001287.6(CLCN7):c.*1157C>T rs9921 0.06755
NM_001287.6(CLCN7):c.1798-10C>T rs35939214 0.03622
NM_001287.6(CLCN7):c.900G>A (p.Ala300=) rs41286695 0.03405
NM_001287.6(CLCN7):c.*1176C>T rs150325021 0.03316
NM_001287.6(CLCN7):c.*990C>T rs114884549 0.03040
NM_001287.6(CLCN7):c.-20G>C rs112055095 0.02459
NM_001287.6(CLCN7):c.801G>A (p.Thr267=) rs61743590 0.01670
NM_001287.6(CLCN7):c.921G>A (p.Gly307=) rs114169064 0.01310
NM_001287.6(CLCN7):c.696C>T (p.Ser232=) rs117183989 0.01006
NM_001287.6(CLCN7):c.*496T>C rs60516531 0.00800
NM_001287.6(CLCN7):c.*1645G>C rs74002247 0.00770
NM_001287.6(CLCN7):c.1617+13G>A rs58998621 0.00586
NM_001287.6(CLCN7):c.*530G>A rs188481235 0.00519
NM_001287.6(CLCN7):c.1961C>T (p.Thr654Met) rs114827619 0.00491
NM_001287.6(CLCN7):c.675+10C>T rs116495246 0.00471
NM_001287.6(CLCN7):c.-32G>A rs141324197 0.00462
NM_001287.6(CLCN7):c.1626G>T (p.Ala542=) rs147838517 0.00437
NM_001287.6(CLCN7):c.1857G>A (p.Pro619=) rs139826207 0.00342
NM_001287.6(CLCN7):c.*262G>A rs572569244 0.00107

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.