ClinVar Miner

Variants studied for age related macular degeneration 7

Included ClinVar conditions (4):
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 association risk factor total
2 0 1 0 0 2 1 6

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic uncertain significance association risk factor total
HTRA1 2 1 0 1 4
DCT 0 0 1 0 1
MC1R 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance association risk factor total
School of Pharmacy, University of Eastern Finland 0 0 2 0 2
OMIM 0 0 0 1 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 1
Fulgent Genetics, Fulgent Genetics 0 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 0 1

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