Variants studied for Hypertrophic cardiomyopathy 12; Dilated cardiomyopathy 1M

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
28	12	199	98	10	344

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
CSRP3	27	12	198	98	10	342
CSRP3, IGSF22, LDHA, LDHAL6A, LDHC, MRGPRX1, MRGPRX2, PTPN5, SPTY2D1, TMEM86A, TSG101, UEVLD, ZDHHC13	1	0	1	0	0	2

Submitter and significance breakdown #

Total submitters: 5

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	28	11	190	97	10	336
Fulgent Genetics, Fulgent Genetics	0	0	33	1	1	35
Department of Pathology and Laboratory Medicine, Sinai Health System	0	1	0	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	1	0	0	1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	1	0	0	1

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