List of variants in gene SLCO1B1 reported as benign for Rotor syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
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_006446.5(SLCO1B1):c.*463A>G	rs4149088	0.38803
NM_006446.5(SLCO1B1):c.*439T>G	rs4149087	0.38797
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.*449A>C	rs11045891	0.11312
NM_006446.5(SLCO1B1):c.411G>A (p.Ser137=)	rs11045818	0.11112
NM_006446.5(SLCO1B1):c.1929A>C (p.Leu643Phe)	rs34671512	0.05414
NM_006446.5(SLCO1B1):c.1248G>A (p.Val416=)	rs11045859	0.02933
NM_006446.5(SLCO1B1):c.*167T>C	rs4149085	0.01882
NM_006446.5(SLCO1B1):c.1086C>T (p.Tyr362=)	rs57040246	0.01802
NM_006446.5(SLCO1B1):c.1200C>G (p.Phe400Leu)	rs59113707	0.01516
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.733A>G (p.Ile245Val)	rs11045852	0.00969
NM_006446.5(SLCO1B1):c.1332-19G>C	rs75563002	0.00862
NM_006446.5(SLCO1B1):c.1495A>G (p.Ile499Val)	rs74064213	0.00823
NM_006446.5(SLCO1B1):c.*121G>C	rs74064260	0.00654
NM_006446.5(SLCO1B1):c.482-11T>C	rs74541382	0.00577
NM_006446.5(SLCO1B1):c.*46T>G	rs71581985	0.00395
NM_006446.5(SLCO1B1):c.664A>G (p.Ile222Val)	rs79135870	0.00350
NM_006446.5(SLCO1B1):c.*40C>G	rs79775553	0.00038
NM_006446.5(SLCO1B1):c.1498-12A>G	rs80208935	0.00028
NM_006446.5(SLCO1B1):c.452A>G (p.Asn151Ser)	rs2306282	0.00009
NM_006446.5(SLCO1B1):c.1007C>G (p.Pro336Arg)	rs72559747	0.00001
NM_006446.5(SLCO1B1):c.727+33C>T	rs2291076

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