ClinVar Miner

List of variants in gene ABCC9 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_020297.4(ABCC9):c.2631G>A (p.Thr877=) rs139408145 0.00386
NM_020297.4(ABCC9):c.2238-1G>A rs141281214 0.00056
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.1200G>A (p.Thr400=) rs150096625 0.00038
NM_020297.4(ABCC9):c.3339T>G (p.Ser1113=) rs138280089 0.00031
NM_020297.4(ABCC9):c.*7G>A rs180770035 0.00029
NM_020297.4(ABCC9):c.1557G>A (p.Glu519=) rs143346402 0.00029
NM_020297.4(ABCC9):c.2262T>C (p.Tyr754=) rs145561881 0.00029
NM_020297.4(ABCC9):c.305T>C (p.Leu102Pro) rs374659816 0.00029
NM_020297.4(ABCC9):c.3288T>C (p.Phe1096=) rs377372612 0.00011
NM_020297.4(ABCC9):c.852T>A (p.Ser284=) rs113562970 0.00010
NM_020297.4(ABCC9):c.1374C>T (p.Val458=) rs200819464 0.00005
NM_020297.4(ABCC9):c.3018G>A (p.Ser1006=) rs1030642418 0.00004
NM_020297.4(ABCC9):c.2199-6T>C rs535477725 0.00001
NM_020297.4(ABCC9):c.1165-7_1165-6dup
NM_020297.4(ABCC9):c.2355A>T (p.Thr785=) rs886038653
NM_020297.4(ABCC9):c.2751A>G (p.Gln917=) rs1285639817
NM_020297.4(ABCC9):c.2867-9dup
NM_020297.4(ABCC9):c.4450-6_4450-5dup
NM_020297.4(ABCC9):c.480G>A (p.Leu160=)

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