Variants studied for melanoma, cutaneous malignant, susceptibility to, 1

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	not provided	total
10	4	107	31	1	4	157

Gene and significance breakdown #

Total genes and gene combinations: 9

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
STK11	7	2	83	6	0	0	98
BRAF	2	2	9	23	1	0	37
LOC130062899, STK11	0	0	12	1	0	0	13
BRAF, LOC126860202	0	0	2	1	0	0	3
POT1	0	0	0	0	0	2	2
BRCA2	0	0	0	0	0	1	1
LOC110806263, TERT	1	0	0	0	0	0	1
MC1R	0	0	0	0	0	1	1
PTEN	0	0	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Baylor Genetics	1	2	92	0	0	0	95
Fulgent Genetics, Fulgent Genetics	0	1	14	31	1	0	47
OMIM	4	0	0	0	0	0	4
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	1	1	1	0	0	0	3
GenomeConnect, ClinGen	0	0	0	0	0	2	2
Juno Genomics, Hangzhou Juno Genomics, Inc	2	0	0	0	0	0	2
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	2	2
Mendelics	1	0	0	0	0	0	1
Division of Medical Oncology, Washington University at Saint Louis	1	0	0	0	0	0	1

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