ClinVar Miner

List of variants studied for autosomal dominant nonsyndromic hearing loss 2A by Juno Genomics, Hangzhou Juno Genomics, Inc

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_004700.4(KCNQ4):c.1668C>G (p.Tyr556Ter)
NM_004700.4(KCNQ4):c.853G>A (p.Gly285Ser) rs28937588
NM_004700.4(KCNQ4):c.882G>A (p.Trp294Ter)

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