ClinVar Miner

List of variants reported as benign for Three Vessel Coronary Disease

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001562.4(IL18):c.-8-919T>C rs360722 0.81651
NM_139027.6(ADAMTS13):c.3910-342A>G rs4962153 0.79091
NM_014272.5(ADAMTS7):c.744A>G (p.Val248=) rs3743057 0.75765
NM_014272.5(ADAMTS7):c.100+3925C>T rs922693 0.70292
NM_139027.6(ADAMTS13):c.2731+77G>A rs652600 0.66100
NM_020469.3(ABO):c.28+1929G>C rs500499 0.47127
NM_139027.6(ADAMTS13):c.2731+739G>T rs671410 0.44413
NM_020469.3(ABO):c.373+163T>C rs2073824 0.39603
NM_020469.3(ABO):c.373+446A>G rs8176731 0.39437
NM_000442.5(PECAM1):c.2008A>G (p.Arg670Gly) rs1131012 0.37733
NM_000442.5(PECAM1):c.1688G>A (p.Ser563Asn) rs12953 0.37617
NM_001562.4(IL18):c.361-1974C>T rs5744280 0.34051
NM_020469.3(ABO):c.29-6479T>A rs8176668 0.33565
NM_014272.5(ADAMTS7):c.640T>C (p.Ser214Pro) rs3825807 0.32795
NM_014272.5(ADAMTS7):c.1322+1499C>T rs11072806 0.32116
NM_004936.4(CDKN2B):c.*2763G>A rs3217992 0.31453
NM_139027.6(ADAMTS13):c.1436-186T>C rs3780809 0.31440
NM_001562.4(IL18):c.105A>C (p.Ser35=) rs549908 0.27313
NM_020469.3(ABO):c.646T>A (p.Phe216Ile) rs8176740 0.25075
NM_004936.4(CDKN2B):c.157-102G>A rs974336 0.14452
NM_020469.3(ABO):c.803G>C (p.Gly268Ala) rs8176747 0.11050
NM_020469.3(ABO):c.203+102C>A rs8176707 0.07289
NM_014272.5(ADAMTS7):c.101-872A>G rs4887112 0.02680
NM_000442.5(PECAM1):c.373G>C (p.Val125Leu) rs281865545
NM_020469.3(ABO):c.29-4774=

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