ClinVar Miner

List of variants in gene LRTOMT, NUMA1 studied for autosomal recessive nonsyndromic hearing loss 63

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_006185.4(NUMA1):c.-109C>T rs114912925 0.02058
NM_006185.4(NUMA1):c.-103+136G>A rs116038324 0.00480
NM_006185.4(NUMA1):c.-103+13G>T rs185830107 0.00021
NM_006185.4(NUMA1):c.-147T>C rs886048621 0.00007
NM_006185.4(NUMA1):c.-103+12G>A rs1944076918
NM_006185.4(NUMA1):c.-103+67G>A rs535003776
NM_006185.4(NUMA1):c.-127A>C rs990462302
NM_006185.4(NUMA1):c.-149G>C rs918454674

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