Variants in gene GPR156 - 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
2	3	64	9	0	76

Condition and significance breakdown #

Total conditions: 4

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	total
not specified	0	0	63	7	70
GPR156-related disorder	0	0	1	2	3
Hearing loss, autosomal recessive 121	2	1	0	0	3
Hearing loss, autosomal recessive	0	2	0	0	2

Submitter and significance breakdown #

Total submitters: 5

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	total
Ambry Genetics	0	0	63	7	70
PreventionGenetics, part of Exact Sciences	0	0	1	2	3
OMIM	2	0	0	0	2
Mustafa Tekin Lab, University Of Miami, Miller School Of Medicine	0	2	0	0	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	0	0	1

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