ClinVar Miner

Variants studied for melanoma, cutaneous malignant, susceptibility to, 5

Included ClinVar conditions (2):
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 risk factor total
0 0 317 135 71 1 484

Gene and significance breakdown #

Total genes and gene combinations: 2
Download table as spreadsheet
Gene or gene combination uncertain significance likely benign benign risk factor total
MC1R 316 135 71 1 483
FANCA, MC1R, SPIRE2, TCF25 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 7
Download table as spreadsheet
Submitter uncertain significance likely benign benign risk factor total
Labcorp Genetics (formerly Invitae), Labcorp 258 103 35 0 396
Illumina Laboratory Services, Illumina 73 36 45 0 154
Fulgent Genetics, Fulgent Genetics 9 5 1 0 15
OMIM 0 0 0 1 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 0 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 1 0 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.