ClinVar Miner

List of variants in gene combination C10orf105, CDH23 reported as pathogenic for auditory system disorder

Included ClinVar conditions (322):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_022124.6(CDH23):c.3481C>T (p.Arg1161Ter) rs397517323
NM_022124.6(CDH23):c.3579+1G>A rs1564759653
NM_022124.6(CDH23):c.4021G>A (p.Asp1341Asn) rs121908351

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