List of variants in gene DEAF1 reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_021008.4(DEAF1):c.56T>C (p.Val19Ala)	rs767318857	0.00124
NM_021008.4(DEAF1):c.1010C>G (p.Pro337Arg)	rs372135504	0.00005
NM_021008.4(DEAF1):c.294G>A (p.Val98=)	rs1038817783
NM_021008.4(DEAF1):c.56_82del (p.Val19_Ala27del)	rs768085739
NM_021008.4(DEAF1):c.56_85del (p.Val19_Ala28del)	rs748949371
NM_021008.4(DEAF1):c.600C>T (p.Asp200=)	rs2133406587

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