ClinVar Miner

Variants studied for alopecia universalis congenita

Included ClinVar conditions (1):
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 total
4 0 105 15 44 167

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign total
HR 4 94 15 42 154
HR, HRURF 0 11 0 2 13

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 103 15 43 161
OMIM 3 1 0 0 4
Genome-Nilou Lab 0 0 0 3 3
Mendelics 1 0 0 0 1
Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University 1 0 0 0 1
3billion 1 0 0 0 1
Department of Human Genetics, Hannover Medical School 0 1 0 0 1

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