ClinVar Miner

Variants studied for Auditory neuropathy spectrum disorder

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
24 7 1 0 0 32

Gene and significance breakdown #

Total genes and gene combinations: 14
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
OTOF 11 3 0 14
AIFM1, RAB33A 1 1 1 3
OPA1 1 1 0 2
SLC52A2 1 1 0 2
TBC1D24 2 0 0 2
CEP135 1 0 0 1
DIAPH1 0 1 0 1
H1-4 1 0 0 1
LOC112840921, OTOF 1 0 0 1
MT-ND6 1 0 0 1
MT-TL1 1 0 0 1
PLP1, RAB9B 1 0 0 1
SLC17A8 1 0 0 1
TUBB4A 1 0 0 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic likely pathogenic uncertain significance total
Department of Otolaryngology, Head and Neck Surgery, Beijing Friendship Hospital, Capital Medical University 24 7 0 31
WangQJ Lab, Chinese People's Liberation Army General Hospital 0 0 1 1

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