ClinVar Miner

List of variants in gene combination LRRC51, LRTOMT reported as uncertain significance for Deafness, autosomal recessive 63

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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NM_001145308.4(LRTOMT):c.-123T>C rs369105155
NM_001145308.4(LRTOMT):c.-149C>T rs145851613
NM_001145308.4(LRTOMT):c.-254G>T rs144139038
NM_001145308.4(LRTOMT):c.-305G>A rs886048627
NM_001145308.4(LRTOMT):c.-322+1G>T rs1565309133
NM_001145308.4(LRTOMT):c.-322+5G>A rs767961368
NM_001145308.4(LRTOMT):c.-344G>A rs886048626
NM_001145308.4(LRTOMT):c.-52G>C rs149637884
NM_001145308.4(LRTOMT):c.-57G>A rs145488053

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