ClinVar Miner

Variants from Retina International

Location: Germany — Primary collection method: not provided
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 not provided total
0 0 0 0 0 1545 1545

Gene and significance breakdown #

Total genes and gene combinations: 22
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Gene or gene combination not provided total
ABCA4 519 519
BEST1 120 120
CDKL5, RS1 108 108
RPGR 103 103
TYR 103 103
RPE65 97 97
PRPH2 86 86
GUCY2D 83 83
CRB1 60 60
GPR143 44 44
CRX 38 38
AIPL1 31 31
GRM6, LOC100130798 28 28
CEP290 23 23
RPGRIP1 21 21
NYX 20 20
RS1 20 20
GRM6 17 17
TULP1 16 16
BEST1, FTH1 5 5
LRAT 2 2
C12orf29, CEP290 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition not provided total
not provided 1545 1545

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