ClinVar Miner

List of variants reported as benign for Dubin-Johnson syndrome by Illumina Laboratory Services, Illumina

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) rs2273697 0.18388
NM_000392.5(ABCC2):c.-24C>T rs717620 0.15338
NM_000392.5(ABCC2):c.4544G>A (p.Cys1515Tyr) rs8187710 0.08637
NM_000392.5(ABCC2):c.4146+11G>C rs17216282 0.05624
NM_000392.5(ABCC2):c.4508+12G>A rs17216212 0.05622
NM_000392.5(ABCC2):c.4290G>T (p.Val1430=) rs1137968 0.05618
NM_000392.5(ABCC2):c.3563T>A (p.Val1188Glu) rs17222723 0.05531
NM_000392.5(ABCC2):c.4488C>T (p.His1496=) rs8187707 0.04774
NM_000392.5(ABCC2):c.2883+11C>T rs41318031 0.04549
NM_000392.5(ABCC2):c.4410G>A (p.Glu1470=) rs8187706 0.03502
NM_000392.5(ABCC2):c.4110C>T (p.Leu1370=) rs7899457 0.03237
NM_000392.5(ABCC2):c.2546T>G (p.Leu849Arg) rs17222617 0.01435
NM_000392.5(ABCC2):c.1446C>G (p.Thr482=) rs113646094 0.01182
NM_000392.5(ABCC2):c.1219C>T (p.Leu407=) rs17216198 0.00876
NM_000392.5(ABCC2):c.2761G>A (p.Gly921Ser) rs41318029 0.00860
NM_000392.5(ABCC2):c.1483A>G (p.Lys495Glu) rs17222561 0.00355
NM_000392.5(ABCC2):c.*201C>T rs150176505 0.00327
NM_000392.5(ABCC2):c.3396T>C (p.Ile1132=) rs17216345 0.00324
NM_000392.5(ABCC2):c.4527C>T (p.Asn1509=) rs8187709 0.00269
NM_000392.5(ABCC2):c.2934G>A (p.Ser978=) rs3740070 0.00080
NM_000392.5(ABCC2):c.2095-6A>G rs202210861 0.00049
NM_000392.5(ABCC2):c.-23G>A rs17216156 0.00038
NM_000392.5(ABCC2):c.1457C>T (p.Thr486Ile) rs17222589 0.00010
NM_000392.5(ABCC2):c.4568A>C (p.Gln1523Pro) rs533470370 0.00002
NM_000392.5(ABCC2):c.1815+4G>A rs574319283 0.00001
NM_000392.5(ABCC2):c.3972C>T (p.Ile1324=) rs3740066

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