ClinVar Miner

List of variants in gene combination ANAPC15, LRTOMT, TOMT reported as pathogenic for autosomal recessive nonsyndromic hearing loss 63

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001393500.2(TOMT):c.515_518dup (p.Ser174fs) rs797044907

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