List of variants in gene DSG2 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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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.3295A>G (p.Thr1099Ala)	rs79068489	0.00137
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr)	rs114544564	0.00130
NM_001943.5(DSG2):c.221A>G (p.His74Arg)	rs201855245	0.00104
NM_001943.5(DSG2):c.*2C>T	rs183494886	0.00054
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro)	rs199681901	0.00038
NM_001943.5(DSG2):c.3266G>A (p.Gly1089Asp)	rs200264407	0.00038
NM_001943.5(DSG2):c.2192A>C (p.Gln731Pro)	rs202063433	0.00032
NM_001943.5(DSG2):c.2334+9G>A	rs776516070	0.00018
NM_001943.5(DSG2):c.1851C>T (p.Leu617=)	rs202057770	0.00017
NM_001943.5(DSG2):c.1847C>T (p.Ala616Val)	rs375527314	0.00006
NM_001943.5(DSG2):c.2340G>T (p.Ala780=)	rs375539435	0.00003
NM_001943.5(DSG2):c.2421G>T (p.Leu807=)	rs374775982	0.00003
NM_001943.5(DSG2):c.84C>G (p.Val28=)	rs397516711	0.00003
NM_001943.5(DSG2):c.1479C>T (p.Asn493=)	rs778100657	0.00001
NM_001943.5(DSG2):c.*9C>T
NM_001943.5(DSG2):c.1280+4AG[3]	rs876657791

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