ClinVar Miner

List of variants in gene ABCC9 reported as benign for Dilated cardiomyopathy 1O

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Total variants: 32
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HGVS dbSNP
NM_005691.3(ABCC9):c.1164+11= rs4762720
NM_005691.3(ABCC9):c.1165-19dup rs35857705
NM_005691.3(ABCC9):c.1165-6del rs35857705
NM_005691.3(ABCC9):c.1296= (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.2093-7T>C rs185235724
NM_005691.3(ABCC9):c.2199-11= rs697250
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2763A>G (p.Leu921=) rs760466255
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
NM_005691.3(ABCC9):c.3267G>A (p.Leu1089=) rs780998911
NM_005691.3(ABCC9):c.3357G>A (p.Leu1119=) rs2287626
NM_005691.3(ABCC9):c.4450-16dup rs4148680
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.817-7del rs193922684
NM_020297.3(ABCC9):c.1056C>T (p.Tyr352=) rs149408382
NM_020297.3(ABCC9):c.1677G>A (p.Ala559=) rs76458291
NM_020297.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_020297.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_020297.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_020297.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_020297.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_020297.3(ABCC9):c.3030T>C (p.Ala1010=) rs76102634
NM_020297.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_020297.3(ABCC9):c.3339T>G (p.Ser1113=) rs138280089
NM_020297.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_020297.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_020297.3(ABCC9):c.3768T>C (p.Leu1256=) rs150303433
NM_020297.3(ABCC9):c.4450-5del rs4148680
NM_020297.3(ABCC9):c.789C>T (p.Cys263=) rs58386780
NM_020297.3(ABCC9):c.798T>C (p.Asp266=) rs138356189
NM_020297.3(ABCC9):c.924T>C (p.Asp308=) rs139127928

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