ClinVar Miner

List of variants reported as not provided for autosomal dominant nonsyndromic deafness 6 by GenomeConnect, ClinGen

Included ClinVar conditions (3):

Cataract 41; Diabetes mellitus AND insipidus with optic atrophy AND deafness; WFS1-Related Disorders; Diabetes mellitus type 2; Wolfram-like syndrome, autosomal dominant
Diabetes mellitus AND insipidus with optic atrophy AND deafness; WFS1-Related Disorders; Wolfram-like syndrome, autosomal dominant
WFS1-Related Disorders

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Total variants: 3

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HGVS	dbSNP
NM_004667.5(HERC2):c.7617+4A>C	rs1567006110
NM_006005.3(WFS1):c.124C>T (p.Arg42Ter)	rs71530923
NM_006005.3(WFS1):c.482G>A (p.Arg161Gln)	rs115346085

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