ClinVar Miner

List of variants in gene combination LRTOMT, NUMA1 reported as uncertain significance for Deafness, autosomal recessive 63

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_001145308.4(LRTOMT):c.-554G>A rs886048622
NM_001145308.4(LRTOMT):c.-705A>G rs886048621
NM_001145308.4(LRTOMT):c.-762C>A rs185830107
NM_001145308.4(LRTOMT):c.-816C>T rs535003776
NM_006185.4(NUMA1):c.-103+12G>A
NM_006185.4(NUMA1):c.-103+136G>A
NM_006185.4(NUMA1):c.-127A>C
NM_006185.4(NUMA1):c.-149G>C

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.