List of variants reported as benign for bilirubin metabolism disease by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_019844.4(SLCO1B3):c.699G>A (p.Met233Ile)	rs7311358	0.71410
NM_019844.4(SLCO1B3):c.360-3C>T	rs3764009	0.71397
NM_019844.4(SLCO1B3):c.1557A>G (p.Ala519=)	rs2053098	0.71374
NM_019844.4(SLCO1B3):c.334T>G (p.Ser112Ala)	rs4149117	0.70446
NM_019844.4(SLCO1B3):c.1833G>A (p.Gly611=)	rs3764006	0.69958
NM_006446.5(SLCO1B1):c.388A>G (p.Asn130Asp)	rs2306283	0.53370
NM_006446.5(SLCO1B1):c.571T>C (p.Leu191=)	rs4149057	0.46746
NM_006446.5(SLCO1B1):c.597C>T (p.Phe199=)	rs2291075	0.44938
NM_019844.4(SLCO1B3):c.-7_-4del	rs4149158	0.23343
NM_019844.4(SLCO1B3):c.-28_-11del	rs527574443	0.23308
NM_006446.5(SLCO1B1):c.463C>A (p.Pro155Thr)	rs11045819	0.12387
NM_006446.5(SLCO1B1):c.521T>C (p.Val174Ala)	rs4149056	0.12106
NM_006446.5(SLCO1B1):c.411G>A (p.Ser137=)	rs11045818	0.11112
NM_019844.4(SLCO1B3):c.767G>C (p.Gly256Ala)	rs60140950	0.10532
NM_006446.5(SLCO1B1):c.1929A>C (p.Leu643Phe)	rs34671512	0.05414
NM_019844.4(SLCO1B3):c.1977G>A (p.Ser659=)	rs60571683	0.03895
NM_006446.5(SLCO1B1):c.1248G>A (p.Val416=)	rs11045859	0.02933
NM_006446.5(SLCO1B1):c.1086C>T (p.Tyr362=)	rs57040246	0.01802
NM_006446.5(SLCO1B1):c.1452C>T (p.Pro484=)	rs74064211	0.01133
NM_006446.5(SLCO1B1):c.882G>A (p.Leu294=)	rs11045854	0.00971
NM_006446.5(SLCO1B1):c.1332-19G>C	rs75563002	0.00862
NM_019844.4(SLCO1B3):c.759T>A (p.Arg253=)	rs61736830	0.00862
NM_006446.5(SLCO1B1):c.482-11T>C	rs74541382	0.00577

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