ClinVar Miner

List of variants in gene MVK reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_000431.4(MVK):c.371+8C>T rs67886029
NM_000431.4(MVK):c.381G>A (p.Pro127=) rs140397628
NM_000431.4(MVK):c.405G>A (p.Ser135=) rs34368092
NM_000431.4(MVK):c.441C>T (p.Ala147=) rs138342076
NM_000431.4(MVK):c.510C>T (p.Asp170=) rs2287218
NM_000431.4(MVK):c.632-18A>G rs2270375
NM_000431.4(MVK):c.677+12del rs774948892
NM_000431.4(MVK):c.78+61A>G rs61940512
NM_000431.4(MVK):c.789C>G (p.Pro263=) rs146181903
NM_000431.4(MVK):c.79-164T>G rs6606734
NM_000431.4(MVK):c.831C>T (p.Arg277=) rs104895353
NM_000431.4(MVK):c.885+24G>A rs2270374

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.