ClinVar Miner

List of variants reported as uncertain significance for autosomal dominant nonsyndromic hearing loss 2A by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Included ClinVar conditions (1):

Autosomal dominant nonsyndromic hearing loss 2A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.28G>A (p.Gly10Ser)
NM_004700.4(KCNQ4):c.331A>G (p.Ser111Gly)
NM_004700.4(KCNQ4):c.670T>C (p.Trp224Arg)
NM_004700.4(KCNQ4):c.785A>T (p.Asp262Val)	rs80358275

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