ClinVar Miner

Variants studied for ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder

Included ClinVar conditions (2):
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
15 1 2 0 1 19

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
ADNP 15 1 2 1 19

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 7 0 0 0 7
GeneReviews 3 0 0 1 4
Laboratoire de Cytogenetique,Hospices Civils de Lyon 3 0 0 0 3
Molecular Genetics Laboratory,BC Children's and BC Women's Hospitals 1 1 0 0 2
Fulgent Genetics 1 0 1 0 2
Groupe Hospitalier Pitie Salpetriere, UF Genomique du Developpement,Assistance Publique Hopitaux de Paris 2 0 0 0 2
Baylor Miraca Genetics Laboratories, 1 0 0 0 1
Illumina Clinical Services Laboratory,Illumina 0 0 1 0 1
HudsonAlpha Institute for Biotechnology 1 0 0 0 1
Center of Genomic medicine, Geneva,University Hospital of Geneva 1 0 0 0 1
Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues 1 0 0 0 1
Undiagnosed Diseases Network,NIH 1 0 0 0 1

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