ClinVar Miner

Variants studied for neurotic disorder

Included ClinVar conditions (8):
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 affects likely risk allele uncertain risk allele total
2 2 3 0 0 1 2 1 11

Gene and significance breakdown #

Total genes and gene combinations: 8
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Gene or gene combination pathogenic likely pathogenic uncertain significance affects likely risk allele uncertain risk allele total
​intergenic 1 0 1 0 0 0 2
MRE11 0 0 2 0 0 0 2
NOTCH3 1 1 0 0 0 0 2
BDNF 0 0 0 0 1 0 1
CACNA1C 0 0 0 0 0 1 1
FKBP5 0 0 0 0 1 0 1
OGDHL 0 0 0 1 0 0 1
TWNK 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance affects likely risk allele uncertain risk allele total
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 1 2 0 0 0 3
Talkowski Laboratory, Center for Human Genetic Research, Massachusetts General Hospital 1 0 1 0 0 0 2
NIHR Bioresource Rare Diseases, University of Cambridge 1 1 0 0 0 0 2
Department of Behavioral Medicine, National Institute of Mental Health, National Center of Neurology and Psychiatry 0 0 0 0 1 1 2
Key Laboratory of Real Time Tracing of Brain Circuits of Neurology and Psychiatry, Nankai University Affiliated Tianjin Fourth Center Hospital 0 0 0 1 0 0 1
Thompson Institute, University of the Sunshine Coast 0 0 0 0 1 0 1

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