ClinVar Miner

List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 49 by King Laboratory, University of Washington

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_001038603.3(MARVELD2):c.608dup (p.Leu203fs) rs2150914115

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