ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic hearing loss 24 by Genome-Nilou Lab

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_002906.4(RDX):c.1587+38T>G rs10450619 0.41780
NM_002906.4(RDX):c.-64-6del rs61003001

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