Variants studied for split hand-foot malformation 4

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
4	5	15	17	0	41

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	total
TP63	4	5	15	17	41

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	total
Fulgent Genetics, Fulgent Genetics	0	0	15	17	32
OMIM	3	0	0	0	3
MGZ Medical Genetics Center	0	1	0	0	1
Illumina Laboratory Services, Illumina	0	0	1	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	0	1	0	0	1
Laboratorio de Genética Hospitales Universitarios Virgen de las Nieves y Clínico San Cecilio (Granada, Spain), Hospitales Universitarios Virgen de las Nieves y Clínico San Cecilio (Granada, Spain)	0	1	0	0	1
Division of Genetics, Dept of Pediatrics, All India Institute of Medical Sciences	0	1	0	0	1
3billion	1	0	0	0	1
McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College	0	1	0	0	1

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