ClinVar Miner

List of variants in gene combination ERCC2, KLC3 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_177417.3(KLC3):c.*101C>G rs3916891

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