Variants in gene DSG2 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.166G>A (p.Val56Met)	rs121913013	0.00150
NM_001943.5(DSG2):c.991G>A (p.Glu331Lys)	rs121913012	0.00002
NM_001943.5(DSG2):c.1520G>A (p.Cys507Tyr)	rs121913009	0.00001
NM_001943.5(DSG2):c.1487dup (p.Cys496fs)	rs730880347
NM_001943.5(DSG2):c.2434G>T (p.Gly812Cys)	rs121913010
NM_001943.5(DSG2):c.3340C>T (p.Gln1114Ter)	rs776078563
NM_001943.5(DSG2):c.829_840del (p.Leu277_Met280del)	rs794728093

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