ClinVar Miner

List of variants in gene ABCC9 reported as benign for cardiomyopathy

Included ClinVar conditions (522):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_020297.4(ABCC9):c.2199-11= rs697250 0.99814
NM_020297.4(ABCC9):c.1296= (p.Pro432=) rs10770865 0.99692
NM_020297.4(ABCC9):c.1164+11= rs4762720 0.98998
NM_020297.4(ABCC9):c.574-5C>A rs3759236 0.59559
NM_020297.4(ABCC9):c.3566+2212G>A rs829069 0.55919
NM_020297.4(ABCC9):c.1912-76A>C rs1283802 0.33920
NM_020297.4(ABCC9):c.2424+9T>C rs11835804 0.02576
NM_020297.4(ABCC9):c.1848C>T (p.Asp616=) rs61001398 0.01493
NM_020297.4(ABCC9):c.3321C>T (p.Ile1107=) rs35404804 0.01226
NM_020297.4(ABCC9):c.789C>T (p.Cys263=) rs58386780 0.01183
NM_020297.4(ABCC9):c.2200G>A (p.Val734Ile) rs61688134 0.00769
NM_020297.4(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473 0.00739
NM_020297.4(ABCC9):c.2643+17G>C rs151310554 0.00584
NM_020297.4(ABCC9):c.2644-19G>A rs73254534 0.00507
NM_020297.4(ABCC9):c.285-16G>A rs144825585 0.00448
NM_020297.4(ABCC9):c.142+15dup rs571187142 0.00428
NM_020297.4(ABCC9):c.2631G>A (p.Thr877=) rs139408145 0.00386
NM_020297.4(ABCC9):c.2523C>T (p.Ala841=) rs144537241 0.00345
NM_020297.4(ABCC9):c.1056C>T (p.Tyr352=) rs149408382 0.00276
NM_020297.4(ABCC9):c.2093-7T>C rs185235724 0.00261
NM_020297.4(ABCC9):c.407-14C>A rs201279882 0.00248
NM_020297.4(ABCC9):c.3768T>C (p.Leu1256=) rs150303433 0.00209
NM_020297.4(ABCC9):c.1677G>A (p.Ala559=) rs76458291 0.00193
NM_020297.4(ABCC9):c.924T>C (p.Asp308=) rs139127928 0.00140
NM_020297.4(ABCC9):c.798T>C (p.Asp266=) rs138356189 0.00113
NM_020297.4(ABCC9):c.2826T>C (p.Tyr942=) rs141025897 0.00092
NM_020297.4(ABCC9):c.2199-13G>A rs201226082 0.00062
NM_020297.4(ABCC9):c.2238-1G>A rs141281214 0.00056
NM_020297.4(ABCC9):c.2770-13A>G rs184123387 0.00055
NM_020297.4(ABCC9):c.372T>C (p.Asn124=) rs377384557 0.00051
NM_020297.4(ABCC9):c.4512+16C>T rs376147813 0.00049
NM_020297.4(ABCC9):c.2862C>T (p.Asp954=) rs2291550 0.00041
NM_020297.4(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226 0.00039
NM_020297.4(ABCC9):c.3030T>C (p.Ala1010=) rs76102634 0.00039
NM_020297.4(ABCC9):c.3339T>G (p.Ser1113=) rs138280089 0.00031
NM_020297.4(ABCC9):c.2262T>C (p.Tyr754=) rs145561881 0.00029
NM_020297.4(ABCC9):c.4450-14T>A rs531295886 0.00016
NM_020297.4(ABCC9):c.96C>T (p.Val32=) rs727505034 0.00011
NM_020297.4(ABCC9):c.3267G>A (p.Leu1089=) rs780998911 0.00009
NM_020297.4(ABCC9):c.1374C>T (p.Val458=) rs200819464 0.00005
NM_020297.4(ABCC9):c.3670-12G>A rs749942631 0.00004
NM_020297.4(ABCC9):c.3357G>A (p.Leu1119=) rs2287626 0.00003
NM_020297.4(ABCC9):c.1165-6del rs35857705
NM_020297.4(ABCC9):c.1165-6dup rs35857705
NM_020297.4(ABCC9):c.142+19T>A rs547603072
NM_020297.4(ABCC9):c.1803-5dup rs761901621
NM_020297.4(ABCC9):c.2238-17del rs4148670
NM_020297.4(ABCC9):c.2238-17dup rs4148670
NM_020297.4(ABCC9):c.2238-18_2238-17del rs4148670
NM_020297.4(ABCC9):c.2644-11G>A rs61926078
NM_020297.4(ABCC9):c.2763A>G (p.Leu921=) rs760466255
NM_020297.4(ABCC9):c.2770-16A>G
NM_020297.4(ABCC9):c.3567-7dup
NM_020297.4(ABCC9):c.3772-16dup
NM_020297.4(ABCC9):c.4450-5del rs4148680
NM_020297.4(ABCC9):c.4450-5dup rs4148680
NM_020297.4(ABCC9):c.4450-6_4450-5del rs4148680
NM_020297.4(ABCC9):c.817-16dup rs193922684
NM_020297.4(ABCC9):c.817-18del rs199947733
NM_020297.4(ABCC9):c.817-18dup rs199947733
NM_020297.4(ABCC9):c.817-7del rs193922684

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