Variants in gene DIAPH1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005219.5(DIAPH1):c.1423G>A (p.Glu475Lys)	rs193036129	0.00123
NM_005219.5(DIAPH1):c.1765_1766dup	rs539203577
NM_005219.5(DIAPH1):c.1769G>T (p.Gly590Val)	rs189809247
NM_005219.5(DIAPH1):c.1821TCC[9] (p.Pro619_Pro620del)	rs3075570
NM_005219.5(DIAPH1):c.402+12del	rs555848272

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