ClinVar Miner

Variants studied for Joubert syndrome and related disorders

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
84 126 0 0 0 210

Gene and significance breakdown #

Total genes and gene combinations: 26
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Gene or gene combination pathogenic likely pathogenic total
CPLANE1 13 13 26
AHI1 14 10 24
TMEM67 12 9 21
RPGRIP1L 4 11 15
INPP5E 3 10 13
CEP104 3 8 11
NPHP1 6 5 11
ARL13B 1 9 10
TMEM231 6 4 10
NPHP3, NPHP3-ACAD11 2 6 8
TCTN1 2 6 8
TCTN2 3 5 8
KIAA0586 4 3 7
KIF14 0 7 7
B9D2 1 4 5
B9D1 0 4 4
TCTN3 4 0 4
TMEM237 1 3 4
LOC130004408, TCTN3 1 2 3
TMEM138 2 1 3
CC2D2A 1 1 2
LOC129937586, NPHP3, NPHP3-ACAD11 0 2 2
CEP104, LOC126805586 0 1 1
CEP290 1 0 1
LRRCC1 0 1 1
NPHP3 0 1 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic likely pathogenic total
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 81 121 202
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 3 4 7
Manipal Hospitals, Manipal Hospital 0 1 1

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