ClinVar Miner

List of variants in gene WWOX reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_016373.3(WWOX):c.107+2_107+5delTAAG rs1555532979
NM_016373.4(WWOX):c.1043del (p.Phe348fs) rs1064795117
NM_016373.4(WWOX):c.172G>A (p.Asp58Asn) rs1131691285
NM_016373.4(WWOX):c.214C>T (p.Gln72Ter) rs201008667
NM_016373.4(WWOX):c.410G>A (p.Gly137Glu) rs761879076
NM_016373.4(WWOX):c.583G>T (p.Glu195Ter) rs1567542020
NM_016373.4(WWOX):c.605+5G>A rs1039151413
NM_016373.4(WWOX):c.749C>G (p.Ser250Ter) rs368928190

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.