ClinVar Miner

List of variants reported as benign for Progressive familial intrahepatic cholestasis 2 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 25
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HGVS dbSNP
NM_003742.4(ABCB11):c.*236A>G rs473351
NM_003742.4(ABCB11):c.*368G>A rs495714
NM_003742.4(ABCB11):c.*420A>G rs496550
NM_003742.4(ABCB11):c.-97T>C rs0
NM_003742.4(ABCB11):c.108T>C (p.Asp36=) rs3815675
NM_003742.4(ABCB11):c.1185G>A (p.Glu395=) rs57509552
NM_003742.4(ABCB11):c.1331T>C (p.Val444Ala) rs2287622
NM_003742.4(ABCB11):c.1605C>T (p.Ala535=) rs144848376
NM_003742.4(ABCB11):c.1636C>A (p.Gln546Lys) rs111482608
NM_003742.4(ABCB11):c.1772A>G (p.Asn591Ser) rs11568367
NM_003742.4(ABCB11):c.2029A>G (p.Met677Val) rs11568364
NM_003742.4(ABCB11):c.2093G>A (p.Arg698His) rs138642043
NM_003742.4(ABCB11):c.2134T>C (p.Leu712=) rs191649793
NM_003742.4(ABCB11):c.2412A>G (p.Ala804=) rs11568373
NM_003742.4(ABCB11):c.2594C>T (p.Ala865Val) rs118109635
NM_003742.4(ABCB11):c.270T>C (p.Phe90=) rs4148777
NM_003742.4(ABCB11):c.3084A>G (p.Ala1028=) rs497692
NM_003742.4(ABCB11):c.3258A>G (p.Thr1086=) rs11568359
NM_003742.4(ABCB11):c.3330G>A (p.Ala1110=) rs113099601
NM_003742.4(ABCB11):c.3556G>A (p.Glu1186Lys) rs1521808
NM_003742.4(ABCB11):c.389+8G>A rs11568363
NM_003742.4(ABCB11):c.402C>T (p.Ile134=) rs11568377
NM_003742.4(ABCB11):c.807T>C (p.Tyr269=) rs2287616
NM_003742.4(ABCB11):c.909-15A>G rs2287618
NM_003742.4(ABCB11):c.957A>G (p.Gly319=) rs7563233

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