List of variants in gene DSG2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 31

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HGVS	dbSNP	gnomAD frequency
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.2368C>T (p.His790Tyr)	rs114544564	0.00130
NM_001943.5(DSG2):c.221A>G (p.His74Arg)	rs201855245	0.00104
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.716T>C (p.Val239Ala)	rs200997703	0.00037
NM_001943.5(DSG2):c.1851C>T (p.Leu617=)	rs202057770	0.00017
NM_001943.5(DSG2):c.545A>G (p.Asn182Ser)	rs368512832	0.00013
NM_001943.5(DSG2):c.1597G>A (p.Val533Ile)	rs199761749	0.00010
NM_001943.5(DSG2):c.2643C>T (p.Thr881=)	rs180695545	0.00010
NM_001943.5(DSG2):c.147C>T (p.Arg49=)	rs531036279	0.00009
NM_001943.5(DSG2):c.3195T>C (p.Thr1065=)	rs544981484	0.00007
NM_001943.5(DSG2):c.3244C>G (p.Pro1082Ala)	rs191300661	0.00007
NM_001943.5(DSG2):c.1089G>A (p.Ser363=)	rs372598337	0.00006
NM_001943.5(DSG2):c.1491C>T (p.Pro497=)	rs587780928	0.00006
NM_001943.5(DSG2):c.1643G>A (p.Arg548His)	rs551034751	0.00006
NM_001943.5(DSG2):c.1847C>T (p.Ala616Val)	rs375527314	0.00006
NM_001943.5(DSG2):c.862G>A (p.Val288Ile)	rs780374242	0.00005
NM_001943.5(DSG2):c.1688T>G (p.Leu563Arg)	rs780469370	0.00004
NM_001943.5(DSG2):c.2328C>A (p.Phe776Leu)	rs771104668	0.00004
NM_001943.5(DSG2):c.2959G>T (p.Val987Phe)	rs141405267	0.00004
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys)	rs576404380	0.00003
NM_001943.5(DSG2):c.3225G>A (p.Thr1075=)	rs773954315	0.00002
NM_001943.5(DSG2):c.3291T>C (p.Asn1097=)	rs757473850	0.00002
NM_001943.5(DSG2):c.1791C>T (p.Ser597=)	rs768167385	0.00001
NM_001943.5(DSG2):c.222T>C (p.His74=)	rs367797047	0.00001
NM_001943.5(DSG2):c.269C>T (p.Thr90Ile)	rs772744115	0.00001
NM_001943.5(DSG2):c.1280+4AG[3]	rs876657791
NM_001943.5(DSG2):c.2235G>A (p.Thr745=)	rs759572082
NM_001943.5(DSG2):c.858C>T (p.Val286=)	rs1555671463

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