ClinVar Miner

Variants studied for candidiasis, familial, 9

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
3 1 359 250 40 651

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 total
IL17RC 3 1 310 239 37 589
IL17RC, LOC129936144 0 0 37 6 1 44
IL17RC, LOC129936143 0 0 9 5 1 14
BRK1, CIDEC, CRELD1, EMC3, FANCD2, FANCD2OS, IL17RC, IL17RE, JAGN1, PRRT3, VHL 0 0 1 0 0 1
CIDEC, CRELD1, EMC3, FANCD2, IL17RC, IL17RE, JAGN1, PRRT3 0 0 1 0 0 1
CRELD1, IL17RC, LOC129936144 0 0 0 0 1 1
IL17RC, IL17RE, JAGN1 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 0 0 358 249 39 646
Genome-Nilou Lab 0 0 0 0 4 4
OMIM 3 0 0 0 0 3
Fulgent Genetics, Fulgent Genetics 0 0 1 1 0 2
Mendelics 0 0 0 0 1 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 1
Al Jalila Children's Genomics Center, Al Jalila Childrens Speciality Hospital 0 0 0 1 0 1
Lifecell International Pvt. Ltd 0 1 0 0 0 1

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