List of variants in gene DSG2 reported by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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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.1332_1354del (p.Ser445_Glu446insTer)	rs2073222422
NM_001943.5(DSG2):c.1385del (p.Asn462fs)	rs2510917341
NM_001943.5(DSG2):c.523+1G>A	rs553299589
NM_001943.5(DSG2):c.523+1G>T	rs553299589

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