List of variants in gene combination LOC107982234, WT1 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.181C>A (p.Arg61=)	rs2234581	0.00269
NM_024426.6(WT1):c.123G>C (p.Pro41=)	rs555140661	0.00189
NM_024426.6(WT1):c.216G>T (p.Gln72His)	rs5030135	0.00036
NM_024426.6(WT1):c.193G>A (p.Gly65Arg)	rs374404615	0.00018
NM_024426.6(WT1):c.381C>G (p.Pro127=)	rs771681406	0.00009

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