C0027708[trait identifier] AND "Color Diagnostics, LLC DBA Color Healt - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 304418	NM_024426.6(WT1):c.1200C>T (p.Tyr400=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +7 more	GConflicting classifications of pathogenicity
Select item 198591	NM_024426.6(WT1):c.1122A>G (p.Arg374=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Meacham syndrome +9 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 provided +10 more	GBenign
Select item 135453	NM_024426.6(WT1):c.760C>T (p.Pro254Ser)	WT1 (P37S +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +11 more	GConflicting classifications of pathogenicity
Select item 261713	NM_024426.6(WT1):c.609C>T (p.Asn203=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +9 more	GBenign
Select item 193454	NM_024426.6(WT1):c.345C>T (p.Pro115=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +9 more	GBenign
Select item 261710	NM_024426.6(WT1):c.213G>T (p.Pro71=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Nephroblastoma +9 more	GBenign
Select item 241476	NM_024426.6(WT1):c.181C>A (p.Arg61=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +10 more	GBenign/Likely benign
Select item 193453	NM_024426.6(WT1):c.123G>C (p.Pro41=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Meacham syndrome +10 more	GBenign/Likely benign
Select item 184326	NM_005359.6(SMAD4):c.875C>T (p.Pro292Leu)	SMAD4 (P292L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity