ClinVar Miner

List of variants reported as benign for autosomal recessive nonsyndromic hearing loss 24 by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_002906.4(RDX):c.-64-6del rs61003001

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