List of variants in gene WT1 reported as uncertain significance for aniridia

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:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1158G>A (p.Ser386=)	rs377446096	0.00009
NM_024426.6(WT1):c.1150G>A (p.Val384Ile)	rs977244044	0.00004
NM_024426.6(WT1):c.1142C>T (p.Pro381Leu)	rs1014605516	0.00003
NM_024426.6(WT1):c.1092C>A (p.His364Gln)	rs587778756	0.00002
NM_024426.6(WT1):c.779C>T (p.Ser260Leu)	rs1444869026	0.00002
NM_024426.6(WT1):c.1253G>T (p.Arg418Met)	rs373176048	0.00001
NM_024426.6(WT1):c.1487A>G (p.Lys496Arg)	rs760370132	0.00001
NM_024426.6(WT1):c.1559T>C (p.Leu520Pro)	rs774228907	0.00001
NM_024426.6(WT1):c.1562C>T (p.Ala521Val)	rs749266841	0.00001
NM_024426.6(WT1):c.685G>A (p.Gly229Arg)	rs767419243	0.00001
NM_024426.6(WT1):c.691C>T (p.Pro231Ser)	rs766425764	0.00001
NM_024426.6(WT1):c.887+19C>G	rs755113185	0.00001
NM_024426.6(WT1):c.1127T>C (p.Val376Ala)	rs1180529775
NM_024426.6(WT1):c.1162T>C (p.Ser388Pro)	rs992930804
NM_024426.6(WT1):c.1218A>C (p.Arg406Ser)	rs1554939793
NM_024426.6(WT1):c.722C>T (p.Ala241Val)	rs1190263054
NM_024426.6(WT1):c.746T>G (p.Phe249Cys)	rs777119782
NM_024426.6(WT1):c.785-14G>A	rs375514482
NM_024426.6(WT1):c.989C>T (p.Ser330Leu)	rs762688982

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