ClinVar Miner

List of variants in gene combination SLCO1B3, SLCO1B3-SLCO1B7 reported as benign for Rotor syndrome

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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_019844.4(SLCO1B3):c.-7_-4del rs4149158 0.23343
NM_019844.4(SLCO1B3):c.-28_-11del rs527574443 0.23308
NM_019844.4(SLCO1B3):c.767G>C (p.Gly256Ala) rs60140950 0.10532
NM_019844.4(SLCO1B3):c.1977G>A (p.Ser659=) rs60571683 0.03895
NM_019844.4(SLCO1B3):c.439A>G (p.Thr147Ala) rs57585902 0.00971
NM_019844.4(SLCO1B3):c.759T>A (p.Arg253=) rs61736830 0.00862
NM_019844.4(SLCO1B3):c.*642G>A rs77957556 0.00684
NM_019844.4(SLCO1B3):c.108C>G (p.Phe36Leu) rs79042365 0.00606
NM_019844.4(SLCO1B3):c.69C>T (p.Arg23=) rs149944473 0.00438
NM_019844.4(SLCO1B3):c.676C>G (p.Leu226Val) rs115227445 0.00361
NM_019844.4(SLCO1B3):c.434A>G (p.Asn145Ser) rs146623116 0.00184
NM_019844.4(SLCO1B3):c.*548A>T rs117703648 0.00136
NM_019844.4(SLCO1B3):c.335C>A (p.Ser112Tyr) rs145334570 0.00052
NM_019844.4(SLCO1B3):c.1857A>T (p.Val619=) rs143827641 0.00051
NM_019844.4(SLCO1B3):c.484T>G (p.Cys162Gly) rs140353351 0.00021
NM_019844.4(SLCO1B3):c.801A>G (p.Leu267=) rs373432026 0.00005
NM_019844.4(SLCO1B3):c.*355dup rs397689574
NM_019844.4(SLCO1B3):c.*627G>A rs79132805

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