C1837026[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 304410	NM_024426.6(WT1):c.*267G>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +5 more	GBenign
Select item 304412	NM_024426.6(WT1):c.*224A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +5 more	GBenign
Select item 304416	NM_024426.6(WT1):c.*88A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +5 more	GBenign
Select item 304417	NM_024426.6(WT1):c.*16G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +5 more	GBenign/Likely benign
Select item 261709	NM_024426.6(WT1):c.1448-49T>C	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +6 more	GBenign
Select item 224479	NM_024426.6(WT1):c.1265-32C>A	WT1	Single nucleotide variant (intron variant)	not specified +6 more	GBenign
Select item 198591	NM_024426.6(WT1):c.1122A>G (p.Arg374=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Nephrotic syndrome, type 4 +8 more	GBenign
Select item 241475	NM_024426.6(WT1):c.1114-9T>C	WT1	Single nucleotide variant (intron variant)	not provided +10 more	GBenign/Likely benign
Select item 261708	NM_024426.6(WT1):c.1074A>G (p.Gln358=)	WT1	Single nucleotide variant (synonymous variant +2 more)	not specified +9 more	GBenign
Select item 261716	NM_024426.6(WT1):c.887+16G>A	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GBenign
Select item 261715	NM_024426.6(WT1):c.785-20G>T	WT1	Single nucleotide variant (intron variant)	not specified +6 more	GBenign/Likely benign
Select item 257619	NM_024426.6(WT1):c.662-1928_662-1927del	LOC107982234, WT1	Deletion (5 prime UTR variant +1 more)	Wilms tumor 1 +6 more	GBenign
Select item 261713	NM_024426.6(WT1):c.609C>T (p.Asn203=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +8 more	GBenign
Select item 261712	NM_024426.6(WT1):c.513C>A (p.Gly171=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign/Likely benign
Select item 193454	NM_024426.6(WT1):c.345C>T (p.Pro115=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign
Select item 241479	NM_024426.6(WT1):c.216G>T (p.Gln72His)	LOC107982234, WT1 (Q72H)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GBenign/Likely benign
Select item 261710	NM_024426.6(WT1):c.213G>T (p.Pro71=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign
Select item 241476	NM_024426.6(WT1):c.181C>A (p.Arg61=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Nephrotic syndrome, type 4 +9 more	GBenign/Likely benign