ClinVar Miner

List of variants in gene ABCB4 reported as likely benign for not specified

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Gene type:
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Total variants: 32
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HGVS dbSNP
NM_000443.3(ABCB4):c.1119+8A>C rs1471180323
NM_000443.3(ABCB4):c.1143A>G (p.Ser381=) rs142671969
NM_000443.3(ABCB4):c.1230+15A>G rs1057522852
NM_000443.3(ABCB4):c.1231-16C>T rs56229233
NM_000443.3(ABCB4):c.1314G>A (p.Thr438=) rs45624933
NM_000443.3(ABCB4):c.1357-17A>G rs201173706
NM_000443.3(ABCB4):c.1560+16A>G rs769175596
NM_000443.3(ABCB4):c.1769G>A (p.Arg590Gln) rs45575636
NM_000443.3(ABCB4):c.1893+6T>C rs8187798
NM_000443.3(ABCB4):c.201C>T (p.His67=) rs747703354
NM_000443.3(ABCB4):c.2325G>A (p.Thr775=) rs8187802
NM_000443.3(ABCB4):c.2394+13G>A rs370406753
NM_000443.3(ABCB4):c.2395-19C>T rs45593648
NM_000443.3(ABCB4):c.2586A>G (p.Ala862=) rs1554400942
NM_000443.3(ABCB4):c.2619T>G (p.Val873=) rs775357102
NM_000443.3(ABCB4):c.3037A>C (p.Arg1013=) rs2230029
NM_000443.3(ABCB4):c.3280-24T>C rs753672621
NM_000443.3(ABCB4):c.3285C>T (p.Leu1095=) rs561612231
NM_000443.3(ABCB4):c.3336C>T (p.Leu1112=) rs756982751
NM_000443.3(ABCB4):c.3381C>T (p.Ala1127=) rs766402494
NM_000443.3(ABCB4):c.3471C>T (p.Ile1157=) rs752578370
NM_000443.3(ABCB4):c.3486+10dupA rs8187809
NM_000443.3(ABCB4):c.3543G>A (p.Gln1181=) rs140592811
NM_000443.3(ABCB4):c.456G>A (p.Lys152=) rs147333055
NM_000443.3(ABCB4):c.523A>G (p.Thr175Ala) rs58238559
NM_000443.3(ABCB4):c.525G>A (p.Thr175=) rs558416191
NM_000443.3(ABCB4):c.536+11T>C rs8187790
NM_000443.3(ABCB4):c.696C>T (p.Ala232=) rs8187791
NM_000443.3(ABCB4):c.807C>T (p.Phe269=) rs1421517860
NM_000443.3(ABCB4):c.996T>C (p.Asn332=) rs1388323440
NM_018849.2(ABCB4):c.1821A>C (p.Val607=)
NM_018849.2(ABCB4):c.712C>G (p.Leu238Val) rs45596335

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