ClinVar Miner

List of variants in gene DSG2 reported as benign for Cardiovascular phenotype

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Total variants: 18
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HGVS dbSNP
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys) rs576404380
NM_001943.5(DSG2):c.1550C>T (p.Ala517Val) rs200509948
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.2137G>A (p.Glu713Lys) rs79241126
NM_001943.5(DSG2):c.217-5G>T rs80073511
NM_001943.5(DSG2):c.2318G>A (p.Arg773Lys) rs2278792
NM_001943.5(DSG2):c.2484T>C (p.Asp828=) rs201051252
NM_001943.5(DSG2):c.2505A>G (p.Thr835=) rs1042769
NM_001943.5(DSG2):c.2587A>C (p.Met863Leu) rs16962093
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.3209C>T (p.Thr1070Met) rs149617776
NM_001943.5(DSG2):c.3243C>T (p.Val1081=) rs11542379
NM_001943.5(DSG2):c.3321T>C (p.Val1107=) rs1791235
NM_001943.5(DSG2):c.473T>G (p.Val158Gly) rs191143292
NM_001943.5(DSG2):c.861C>T (p.Asn287=) rs2230233
NM_001943.5(DSG2):c.877A>G (p.Ile293Val) rs2230234

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