Variants in gene DEAF1 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_021008.4(DEAF1):c.716A>G (p.Glu239Gly)	rs1064795812	0.00001
NM_021008.4(DEAF1):c.1090_1091del (p.Pro365fs)	rs756419434
NM_021008.4(DEAF1):c.641T>C (p.Leu214Pro)	rs1590017658
NM_021008.4(DEAF1):c.646A>G (p.Lys216Glu)	rs1590017652
NM_021008.4(DEAF1):c.658G>A (p.Gly220Ser)	rs751569402
NM_021008.4(DEAF1):c.791A>C (p.Gln264Pro)	rs587777407
NM_021008.4(DEAF1):c.837C>G (p.Cys279Trp)
NM_021008.4(DEAF1):c.890T>C (p.Phe297Ser)	rs1390761338

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