Variants studied for Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome

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)

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
72	11	742	557	37	2	1419

Gene and significance breakdown #

Total genes and gene combinations: 4

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
WT1	51	10	345	337	25	1	768
LOC107982234, WT1	18	1	397	220	12	1	648
LOC106707172, LOC107982234, LOC130005479, WT1	2	0	0	0	0	0	2
DCDC1, DNAJC24, ELP4, IMMP1L, PAX6, RCN1, WT1	1	0	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 2

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Labcorp Genetics (formerly Invitae), Labcorp	72	11	742	557	37	0	1419
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	2	2

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