Database of Pathogenic Variants
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Disease Detail
Disease Name
Deafness, autosomal dominant, 6
OMIM:600965
MedGen:C1833021
Associated Genes and Variants
WFS1
NM_006005.3:c.1480G>A
NM_006005.3:c.2389G>A
NM_006005.3:c.2507A>C
NM_006005.3:c.2576G>C
NM_006005.3:c.2590G>A