Variants in gene ARF1 - ClinVar Miner

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
0	1	0	0	0	1

Condition and significance breakdown #

Total conditions: 1

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Condition	likely pathogenic	total
Periventricular nodular heterotopia 8	1	1

Submitter and significance breakdown #

Total submitters: 2

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Submitter	likely pathogenic	total
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München	1	1
Groupe Hospitalier Pitie Salpetriere, UF Genomique du Developpement, Assistance Publique Hopitaux de Paris	1	1

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