Variants studied for autoimmune thyroid disease, susceptibility to

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	risk factor	total
3	2	19	1	0	5	30

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	risk factor	total
TG	3	2	16	1	4	26
ZFAT	0	0	2	0	1	3
SLA, TG	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 7

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	risk factor	total
Fulgent Genetics, Fulgent Genetics	2	1	16	1	0	20
OMIM	0	0	0	0	5	5
Baylor Genetics	1	0	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	0	1	0	0	1
Genetics and Molecular Pathology, SA Pathology	0	0	1	0	0	1
Yale Center for Mendelian Genomics, Yale University	0	1	0	0	0	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	0	1

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