ClinVar Miner

Variants from INSERM U1051, Institut des Neurosciences de Montpellier

Location: France  Primary collection method: research
Minimum submission review status: Collection method:
Minimum conflict level:
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
15 14 9 0 0 38

Gene and significance breakdown #

Total genes and gene combinations: 20
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
CRB1 2 2 1 5
EYS 3 1 0 4
USH2A 1 2 1 4
CNGB1 1 1 1 3
PCARE 1 2 0 3
TULP1 0 2 1 3
CDHR1 0 0 2 2
PRPF31 1 1 0 2
CERKL 0 0 1 1
EYS, PHF3 0 1 0 1
LCA5 1 0 0 1
LOC122152296, USH2A 0 1 0 1
LOC125371495, NDUFA13 1 0 0 1
LOC126860392, RP1 1 0 0 1
MERTK 1 0 0 1
PRPF8 0 1 0 1
RHO 1 0 0 1
RP1 1 0 0 1
RPE65 0 0 1 1
SNRNP200 0 0 1 1

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic likely pathogenic uncertain significance total
Retinitis pigmentosa 14 14 9 37
Mitochondrial complex I deficiency 1 0 0 1

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