ClinVar Miner

Variants studied for Cone-Rod Dystrophy, Recessive

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 0 291 97 22 410

Gene and significance breakdown #

Total genes and gene combinations: 7
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Gene or gene combination uncertain significance likely benign benign total
CDHR1 104 15 7 126
ABCA4 43 53 7 103
PDE6C 39 5 4 48
RPGRIP1 29 9 2 40
SEMA4A 30 5 1 36
ADAM9 26 3 1 30
C8orf37 20 7 0 27

Submitter and significance breakdown #

Total submitters: 1
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 291 97 22 410

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