List of variants in gene SLCO1B1 reported as likely 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_006446.5(SLCO1B1):c.1200C>G (p.Phe400Leu)	rs59113707	0.01516
NM_006446.5(SLCO1B1):c.*575G>A	rs61760249	0.01303
NM_006446.5(SLCO1B1):c.1463G>C (p.Gly488Ala)	rs59502379	0.01105
NM_006446.5(SLCO1B1):c.733A>G (p.Ile245Val)	rs11045852	0.00969
NM_006446.5(SLCO1B1):c.728-17_728-14del	rs150936610	0.00968
NM_006446.5(SLCO1B1):c.481+1G>T	rs77271279	0.00934
NM_006446.5(SLCO1B1):c.1495A>G (p.Ile499Val)	rs74064213	0.00823
NM_006446.5(SLCO1B1):c.1747+9A>G	rs71577817	0.00351
NM_006446.5(SLCO1B1):c.1332-14T>C	rs71581991	0.00150
NM_006446.5(SLCO1B1):c.*328A>G	rs4149086	0.00042
NM_006446.5(SLCO1B1):c.1331+9A>G	rs76647672	0.00034
NM_006446.5(SLCO1B1):c.210C>T (p.Asp70=)	rs148697674	0.00024
NM_006446.5(SLCO1B1):c.1794G>A (p.Thr598=)	rs201556175	0.00003
NM_006446.5(SLCO1B1):c.633A>G (p.Ile211Met)	rs201722521	0.00003
NM_006446.5(SLCO1B1):c.1812C>T (p.Thr604=)	rs779508352	0.00001
NM_006446.5(SLCO1B1):c.79T>C (p.Leu27=)	rs190581845	0.00001
NM_006446.5(SLCO1B1):c.*134A>T	rs567678480
NM_006446.5(SLCO1B1):c.-3A>G

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