Variants in gene DEAF1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_021008.4(DEAF1):c.1634C>G (p.Ala545Gly)	rs34114147	0.00680
NM_021008.4(DEAF1):c.825C>T (p.His275=)	rs144498322	0.00310
NM_021008.4(DEAF1):c.727A>G (p.Met243Val)	rs71469813	0.00284
NM_021008.4(DEAF1):c.162G>C (p.Ser54=)	rs141389829	0.00133
NM_021008.4(DEAF1):c.231C>T (p.Asp77=)	rs371538775	0.00130
NM_021008.4(DEAF1):c.517+8G>A	rs369913079	0.00048
NM_021008.4(DEAF1):c.855C>T (p.Cys285=)	rs373861624	0.00036
NM_021008.4(DEAF1):c.1182C>T (p.Tyr394=)	rs202179285	0.00014
NM_021008.4(DEAF1):c.1114G>A (p.Ala372Thr)	rs371467345	0.00001

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