ClinVar Miner

List of variants in gene DSG2 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
Download table as spreadsheet
HGVS dbSNP
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly) rs139326669
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile) rs193922639
NM_001943.5(DSG2):c.1284T>C (p.Tyr428=) rs202095254
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn) rs370509593
NM_001943.5(DSG2):c.1317T>C (p.Ser439=) rs727505064
NM_001943.5(DSG2):c.1550C>T (p.Ala517Val) rs200509948
NM_001943.5(DSG2):c.1652-12C>T rs140850369
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013
NM_001943.5(DSG2):c.1724A>G (p.Asn575Ser) rs727502988
NM_001943.5(DSG2):c.1851C>T (p.Leu617=) rs202057770
NM_001943.5(DSG2):c.1911C>T (p.Cys637=) rs201654341
NM_001943.5(DSG2):c.1914A>G (p.Gly638=) rs200395484
NM_001943.5(DSG2):c.2085G>A (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.2100C>T (p.Ser700=) rs397516704
NM_001943.5(DSG2):c.2127T>C (p.His709=) rs876657457
NM_001943.5(DSG2):c.216+14_216+15del rs876657458
NM_001943.5(DSG2):c.221A>G (p.His74Arg) rs201855245
NM_001943.5(DSG2):c.222T>C (p.His74=) rs367797047
NM_001943.5(DSG2):c.2234C>T (p.Thr745Met) rs727504783
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr) rs114544564
NM_001943.5(DSG2):c.2643C>T (p.Thr881=) rs180695545
NM_001943.5(DSG2):c.2759T>G (p.Val920Gly) rs142841727
NM_001943.5(DSG2):c.2886T>G (p.Ile962Met) rs79229040
NM_001943.5(DSG2):c.291A>C (p.Pro97=) rs727502983
NM_001943.5(DSG2):c.3082G>A (p.Gly1028Ser) rs150864240
NM_001943.5(DSG2):c.3198A>G (p.Glu1066=) rs727504601
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met) rs149617776
NM_001943.5(DSG2):c.3244C>G (p.Pro1082Ala) rs191300661
NM_001943.5(DSG2):c.3295A>G (p.Thr1099Ala) rs79068489
NM_001943.5(DSG2):c.474G>A (p.Val158=) rs397516708
NM_001943.5(DSG2):c.545A>G (p.Asn182Ser) rs368512832
NM_001943.5(DSG2):c.618T>A (p.Ala206=) rs397516710
NM_001943.5(DSG2):c.6G>A (p.Ala2=) rs368809971
NM_001943.5(DSG2):c.782G>A (p.Arg261His) rs727502984
NM_001943.5(DSG2):c.829-4G>A rs376424003
NM_001943.5(DSG2):c.84C>G (p.Val28=) rs397516711
NM_001943.5(DSG2):c.852T>C (p.Asn284=) rs62095193

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.