ClinVar Miner

Variants studied for Nonsyndromic Hearing Loss, Dominant

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

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
0 0 638 512 109 1259

Gene and significance breakdown #

Total genes and gene combinations: 21
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Gene or gene combination uncertain significance likely benign benign total
MYH9 50 69 23 142
MYO7A 77 55 10 142
MYH14 73 40 8 121
WFS1 47 50 13 110
MYO6 50 49 4 103
COL11A2 23 60 15 98
TECTA 67 27 4 98
MYO1A 42 19 0 61
TJP2 32 27 1 60
SLC17A8 35 14 1 50
GJB3 19 16 11 46
GJB2 8 22 12 42
SIX1 16 17 3 36
EYA4, TARID 23 10 0 33
TMC1 16 13 3 32
GJB6 26 4 0 30
EYA4 13 4 0 17
COCH, LOC100506071 9 6 1 16
POU4F3 9 3 0 12
COCH 3 6 0 9
LOC112695089, MYH9 0 1 0 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 638 512 109 1259

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