ClinVar Miner

Variants studied for Congenital Stationary Night Blindness, 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 0 260 68 27 355

Gene and significance breakdown #

Total genes and gene combinations: 7
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Gene or gene combination uncertain significance likely benign benign total
GPR179 75 19 3 97
CABP4 67 9 8 84
TRPM1 49 14 6 69
SLC24A1 38 9 1 48
LRIT3 23 13 9 45
DENND4A, SLC24A1 7 3 0 10
LRIT3, RRH 1 1 0 2

Submitter and significance breakdown #

Total submitters: 1
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 260 68 27 355

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