ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic deafness 24 by OMIM

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_001260494.1(RDX):c.60-5775C>T rs121918380
NM_001260496.1(RDX):c.405-1415dup
NM_002906.3(RDX):c.1732G>A (p.Asp578Asn) rs121918379
NM_002906.3(RDX):c.698+1G>A

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