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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.2759T>G (p.Val920Gly)	rs142841727	0.00439
NM_001943.5(DSG2):c.2484T>C (p.Asp828=)	rs201051252	0.00217
NM_001943.5(DSG2):c.1550C>T (p.Ala517Val)	rs200509948	0.00184
NM_001943.5(DSG2):c.166G>A (p.Val56Met)	rs121913013	0.00150
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro)	rs199681901	0.00038
NM_001943.5(DSG2):c.2334+9G>A	rs776516070	0.00018
NM_001943.5(DSG2):c.2643C>T (p.Thr881=)	rs180695545	0.00010
NM_001943.5(DSG2):c.1847C>T (p.Ala616Val)	rs375527314	0.00006
NM_001943.5(DSG2):c.1688T>G (p.Leu563Arg)	rs780469370	0.00004
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn)	rs370509593	0.00003
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys)	rs576404380	0.00003

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