ClinVar Miner

Variants studied for Renal cell carcinoma

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

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
5 2 2024 1232 60 2 3322

Gene and significance breakdown #

Total genes and gene combinations: 7
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
MET 3 2 2020 1232 59 2 3315
CAV1, MET 0 0 2 0 0 0 2
ASZ1, CAPZA2, CFTR, MET, RNU2-1, ST7, ST7-OT3, ST7-OT4, WNT2 0 0 1 0 0 0 1
COMETT, MET 0 0 0 0 1 0 1
MITF 0 0 1 0 0 0 1
SDHB 1 0 0 0 0 0 1
TFE3 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 3 1 2023 1232 59 0 3318
Mendelics 0 0 0 0 3 0 3
Dubai Health Genomic Medicine Center, Dubai Health 1 1 0 0 0 0 2
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 2 2
Clinical Genetics Laboratory, Skane University Hospital Lund 0 0 1 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 1 0 0 0 0 0 1

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