ClinVar Miner

List of variants in gene ABCC9 reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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NM_005691.3(ABCC9):c.1056C>T (p.Tyr352=) rs149408382
NM_005691.3(ABCC9):c.1296= (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1677G>A (p.Ala559=) rs76458291
NM_005691.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_005691.3(ABCC9):c.2644-11G>A rs61926078
NM_005691.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_005691.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_005691.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_005691.3(ABCC9):c.3768T>C (p.Leu1256=) rs150303433
NM_005691.3(ABCC9):c.4450-16dup rs4148680
NM_005691.3(ABCC9):c.574-5= rs3759236
NM_005691.3(ABCC9):c.574-5C>A rs3759236
NM_005691.3(ABCC9):c.789C>T (p.Cys263=) rs58386780
NM_005691.3(ABCC9):c.798T>C (p.Asp266=) rs138356189
NM_005691.3(ABCC9):c.924T>C (p.Asp308=) rs139127928
NM_020297.3(ABCC9):c.1164+11A>G rs4762720
NM_020297.3(ABCC9):c.2199-11T>C rs697250

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