ClinVar Miner

List of variants in gene ABCC2 reported as benign for Dubin-Johnson syndrome

Included ClinVar conditions (1):
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Total variants: 27
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HGVS dbSNP
NM_000392.5(ABCC2):c.*201C>T
NM_000392.5(ABCC2):c.-23G>A
NM_000392.5(ABCC2):c.-24C>T rs717620
NM_000392.5(ABCC2):c.116A>T (p.Tyr39Phe) rs927344
NM_000392.5(ABCC2):c.1219C>T (p.Leu407=) rs17216198
NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) rs2273697
NM_000392.5(ABCC2):c.1446C>G (p.Thr482=) rs113646094
NM_000392.5(ABCC2):c.1457C>T (p.Thr486Ile) rs17222589
NM_000392.5(ABCC2):c.1483A>G (p.Lys495Glu) rs17222561
NM_000392.5(ABCC2):c.1815+4G>A rs574319283
NM_000392.5(ABCC2):c.2095-6A>G rs202210861
NM_000392.5(ABCC2):c.2546T>G (p.Leu849Arg) rs17222617
NM_000392.5(ABCC2):c.2761G>A (p.Gly921Ser) rs41318029
NM_000392.5(ABCC2):c.2883+11C>T rs41318031
NM_000392.5(ABCC2):c.2934G>A (p.Ser978=) rs3740070
NM_000392.5(ABCC2):c.3396T>C (p.Ile1132=) rs17216345
NM_000392.5(ABCC2):c.3563T>A (p.Val1188Glu) rs17222723
NM_000392.5(ABCC2):c.3972C>T (p.Ile1324=) rs3740066
NM_000392.5(ABCC2):c.4110C>T (p.Leu1370=) rs7899457
NM_000392.5(ABCC2):c.4146+11G>C rs17216282
NM_000392.5(ABCC2):c.4290G>T (p.Val1430=) rs1137968
NM_000392.5(ABCC2):c.4410G>A (p.Glu1470=) rs8187706
NM_000392.5(ABCC2):c.4488C>T (p.His1496=) rs8187707
NM_000392.5(ABCC2):c.4508+12G>A rs17216212
NM_000392.5(ABCC2):c.4527C>T (p.Asn1509=) rs8187709
NM_000392.5(ABCC2):c.4544G>A (p.Cys1515Tyr) rs8187710
NM_000392.5(ABCC2):c.4568A>C (p.Gln1523Pro) rs533470370

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