ClinVar Miner

List of variants reported as uncertain significance for Dubin-Johnson syndrome

Included ClinVar conditions (1):
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Total variants: 49
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HGVS dbSNP
NM_000392.5(ABCC2):c.*116del rs777704351
NM_000392.5(ABCC2):c.*259G>T rs138578110
NM_000392.5(ABCC2):c.-43A>G rs765935481
NM_000392.5(ABCC2):c.1008G>A (p.Thr336=) rs761197359
NM_000392.5(ABCC2):c.1032-14C>A rs754368880
NM_000392.5(ABCC2):c.1032-3C>T rs139800035
NM_000392.5(ABCC2):c.108C>T (p.Pro36=) rs886046617
NM_000392.5(ABCC2):c.1209+15G>A rs886046618
NM_000392.5(ABCC2):c.1233C>T (p.Ala411=) rs886046619
NM_000392.5(ABCC2):c.1250T>C (p.Val417Ala) rs199595780
NM_000392.5(ABCC2):c.1325G>A (p.Trp442Ter)
NM_000392.5(ABCC2):c.1346T>C (p.Val449Ala) rs71488021
NM_000392.5(ABCC2):c.150C>T (p.His50=) rs200595851
NM_000392.5(ABCC2):c.159A>G (p.Lys53=) rs17222596
NM_000392.5(ABCC2):c.1602G>T (p.Lys534Asn) rs149593061
NM_000392.5(ABCC2):c.1815+4G>A rs574319283
NM_000392.5(ABCC2):c.1860T>A (p.Asp620Glu) rs141413284
NM_000392.5(ABCC2):c.2095-6A>G rs202210861
NM_000392.5(ABCC2):c.2273G>T (p.Gly758Val) rs786205465
NM_000392.5(ABCC2):c.2362_2363del (p.Leu788fs) rs772673105
NM_000392.5(ABCC2):c.2588T>C (p.Leu863Pro) rs201820826
NM_000392.5(ABCC2):c.2613A>G (p.Glu871=) rs76302654
NM_000392.5(ABCC2):c.2743C>T (p.Arg915Cys) rs112758556
NM_000392.5(ABCC2):c.2747+5G>A rs138988852
NM_000392.5(ABCC2):c.2755T>A (p.Ser919Thr) rs775944091
NM_000392.5(ABCC2):c.2997G>A (p.Trp999Ter) rs572224582
NM_000392.5(ABCC2):c.3008G>T (p.Trp1003Leu) rs147566977
NM_000392.5(ABCC2):c.3068G>T (p.Arg1023Ile) rs374311166
NM_000392.5(ABCC2):c.3104-1G>A rs1054194575
NM_000392.5(ABCC2):c.3239T>C (p.Ile1080Thr) rs138221862
NM_000392.5(ABCC2):c.3256G>A (p.Gly1086Ser) rs769152380
NM_000392.5(ABCC2):c.33+13A>G rs368321703
NM_000392.5(ABCC2):c.3357C>T (p.Ala1119=) rs376532575
NM_000392.5(ABCC2):c.3492C>T (p.Ser1164=) rs144192700
NM_000392.5(ABCC2):c.3500T>C (p.Val1167Ala) rs140680467
NM_000392.5(ABCC2):c.3576C>G (p.Thr1192=) rs146575217
NM_000392.5(ABCC2):c.3648C>A (p.Asn1216Lys) rs144967259
NM_000392.5(ABCC2):c.3815T>C (p.Ile1272Thr) rs886046620
NM_000392.5(ABCC2):c.3888C>G (p.Ser1296Arg) rs143990242
NM_000392.5(ABCC2):c.3973G>A (p.Gly1325Ser) rs759452729
NM_000392.5(ABCC2):c.3988-15G>C rs746609972
NM_000392.5(ABCC2):c.411del (p.Leu138fs) rs1564670777
NM_000392.5(ABCC2):c.4447T>G (p.Phe1483Val) rs886046621
NM_000392.5(ABCC2):c.4454A>G (p.His1485Arg) rs780026074
NM_000392.5(ABCC2):c.4509-9T>C rs180717330
NM_000392.5(ABCC2):c.577-11G>T rs200883270
NM_000392.5(ABCC2):c.57G>A (p.Pro19=) rs772618481
NM_000392.5(ABCC2):c.732G>A (p.Thr244=) rs754060673
NM_000392.5(ABCC2):c.764G>A (p.Arg255Gln) rs139964853

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