ClinVar Miner

List of variants reported as likely benign for arrhythmogenic right ventricular dysplasia 10

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 53
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HGVS dbSNP
NM_001943.5(DSG2):c.1038G>A (p.Lys346=) rs1555627111
NM_001943.5(DSG2):c.1089G>A (p.Ser363=) rs372598337
NM_001943.5(DSG2):c.1110T>C (p.Pro370=) rs772805008
NM_001943.5(DSG2):c.1280+4AG[3] rs876657791
NM_001943.5(DSG2):c.1280+8A>G rs377662063
NM_001943.5(DSG2):c.1281-5G>T rs1280409009
NM_001943.5(DSG2):c.1284T>C (p.Tyr428=) rs202095254
NM_001943.5(DSG2):c.1479C>T (p.Asn493=) rs778100657
NM_001943.5(DSG2):c.147C>T (p.Arg49=) rs531036279
NM_001943.5(DSG2):c.1491C>T (p.Pro497=) rs587780928
NM_001943.5(DSG2):c.1597G>A (p.Val533Ile) rs199761749
NM_001943.5(DSG2):c.159C>T (p.Thr53=) rs959566645
NM_001943.5(DSG2):c.15G>C (p.Pro5=) rs772663614
NM_001943.5(DSG2):c.1652-8C>T rs770497608
NM_001943.5(DSG2):c.1656C>T (p.Thr552=) rs756426150
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013
NM_001943.5(DSG2):c.1688T>G (p.Leu563Arg) rs780469370
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro) rs199681901
NM_001943.5(DSG2):c.1847C>T (p.Ala616Val) rs375527314
NM_001943.5(DSG2):c.1848G>T (p.Ala616=) rs372349945
NM_001943.5(DSG2):c.1851C>T (p.Leu617=) rs202057770
NM_001943.5(DSG2):c.1920C>T (p.Gly640=) rs775642244
NM_001943.5(DSG2):c.2085G>A (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.2085G>C (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.210T>C (p.Ile70=) rs202202636
NM_001943.5(DSG2):c.2192A>C (p.Gln731Pro) rs202063433
NM_001943.5(DSG2):c.221A>G (p.His74Arg) rs201855245
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr) rs114544564
NM_001943.5(DSG2):c.2470C>T (p.Arg824Cys) rs201845396
NM_001943.5(DSG2):c.273A>G (p.Gly91=) rs376944801
NM_001943.5(DSG2):c.2751G>A (p.Ala917=) rs763063602
NM_001943.5(DSG2):c.2780C>T (p.Pro927Leu) rs146402368
NM_001943.5(DSG2):c.2906C>T (p.Ala969Val) rs373598034
NM_001943.5(DSG2):c.2913T>G (p.Ala971=) rs200793530
NM_001943.5(DSG2):c.2997G>A (p.Ser999=) rs763888499
NM_001943.5(DSG2):c.3228G>A (p.Val1076=) rs373966845
NM_001943.5(DSG2):c.3266G>A (p.Gly1089Asp) rs200264407
NM_001943.5(DSG2):c.3336T>G (p.Thr1112=) rs1555628388
NM_001943.5(DSG2):c.3354C>G (p.Ser1118=) rs879254344
NM_001943.5(DSG2):c.42C>T (p.Leu14=) rs1555669691
NM_001943.5(DSG2):c.45+9C>G rs376573409
NM_001943.5(DSG2):c.45+9C>T rs376573409
NM_001943.5(DSG2):c.573C>G (p.Thr191=) rs769514389
NM_001943.5(DSG2):c.57C>T (p.Asn19=) rs587780925
NM_001943.5(DSG2):c.6G>A (p.Ala2=) rs368809971
NM_001943.5(DSG2):c.706A>G (p.Thr236Ala) rs727502985
NM_001943.5(DSG2):c.716T>C (p.Val239Ala) rs200997703
NM_001943.5(DSG2):c.783T>A (p.Arg261=) rs369869320
NM_001943.5(DSG2):c.795C>G (p.Val265=) rs771324254
NM_001943.5(DSG2):c.829-4G>A rs376424003
NM_001943.5(DSG2):c.852T>C (p.Asn284=) rs62095193
NM_001943.5(DSG2):c.915T>C (p.Asn305=) rs1484918582
NM_001943.5(DSG2):c.942A>G (p.Ser314=) rs780279875

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