ClinVar Miner

List of variants in gene combination SLCO1B3, SLCO1B3-SLCO1B7 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_019844.4(SLCO1B3):c.1855G>A (p.Val619Ile) rs202234562 0.00105
NM_019844.4(SLCO1B3):c.645A>G (p.Ile215Met) rs142673817 0.00097
NM_019844.4(SLCO1B3):c.*622G>A rs555196020 0.00083
NM_019844.4(SLCO1B3):c.*509T>C rs554075376 0.00065
NM_019844.4(SLCO1B3):c.1593A>G (p.Thr531=) rs142694767 0.00060
NM_019844.4(SLCO1B3):c.1366C>T (p.Leu456Phe) rs61736817 0.00050
NM_019844.4(SLCO1B3):c.988A>G (p.Lys330Glu) rs146780296 0.00045
NM_019844.4(SLCO1B3):c.*540G>A rs758379038 0.00031
NM_019844.4(SLCO1B3):c.727+10A>G rs201736270 0.00029
NM_019844.4(SLCO1B3):c.1865+11G>A rs376331163 0.00026
NM_019844.4(SLCO1B3):c.*641C>T rs1024598614 0.00024
NM_019844.4(SLCO1B3):c.853_856del (p.Lys285fs) rs554933268 0.00016
NM_019844.4(SLCO1B3):c.592G>A (p.Asp198Asn) rs368649517 0.00015
NM_019844.4(SLCO1B3):c.*562G>T rs545934577 0.00014
NM_019844.4(SLCO1B3):c.1332-15A>G rs201114863 0.00014
NM_019844.4(SLCO1B3):c.404C>T (p.Ser135Leu) rs150039066 0.00013
NM_019844.4(SLCO1B3):c.413G>T (p.Ser138Ile) rs369529563 0.00013
NM_019844.4(SLCO1B3):c.971-2A>G rs140033394 0.00012
NM_019844.4(SLCO1B3):c.542G>A (p.Arg181His) rs180875376 0.00010
NM_019844.4(SLCO1B3):c.*610A>G rs751963988 0.00009
NM_019844.4(SLCO1B3):c.1272A>G (p.Leu424=) rs4149143 0.00009
NM_019844.4(SLCO1B3):c.*362A>C rs1005654068 0.00008
NM_019844.4(SLCO1B3):c.459A>G (p.Thr153=) rs370334648 0.00008
NM_019844.4(SLCO1B3):c.1101C>T (p.Tyr367=) rs777458586 0.00007
NM_019844.4(SLCO1B3):c.*8T>C rs372418887 0.00006
NM_019844.4(SLCO1B3):c.1135+8A>G rs372493449 0.00006
NM_019844.4(SLCO1B3):c.1217G>A (p.Gly406Glu) rs374932005 0.00006
NM_019844.4(SLCO1B3):c.1308C>T (p.Ala436=) rs147428265 0.00006
NM_019844.4(SLCO1B3):c.1074C>T (p.Tyr358=) rs145036538 0.00005
NM_019844.4(SLCO1B3):c.*136C>T rs766036895 0.00004
NM_019844.4(SLCO1B3):c.176T>C (p.Phe59Ser) rs778668812 0.00004
NM_019844.4(SLCO1B3):c.26A>C (p.Lys9Thr) rs200793002 0.00004
NM_019844.4(SLCO1B3):c.99C>T (p.Ala33=) rs144143469 0.00004
NM_019844.4(SLCO1B3):c.*307T>C rs886049140 0.00003
NM_019844.4(SLCO1B3):c.973T>A (p.Phe325Ile) rs775841876 0.00003
NM_019844.4(SLCO1B3):c.1747+5G>A rs748582575 0.00002
NM_019844.4(SLCO1B3):c.471A>G (p.Ile157Met) rs748685876 0.00002
NM_019844.4(SLCO1B3):c.1004A>G (p.Asn335Ser) rs886049136 0.00001
NM_019844.4(SLCO1B3):c.148A>G (p.Ile50Val) rs761530247 0.00001
NM_019844.4(SLCO1B3):c.1741A>G (p.Thr581Ala) rs779952599 0.00001
NM_019844.4(SLCO1B3):c.1747+3A>G rs533193038 0.00001
NM_019844.4(SLCO1B3):c.557C>A (p.Thr186Asn) rs775442032 0.00001
NM_019844.4(SLCO1B3):c.712G>A (p.Gly238Arg) rs747595430 0.00001
NM_019844.4(SLCO1B3):c.757C>T (p.Arg253Cys) rs767676951 0.00001
NM_019844.4(SLCO1B3):c.*219G>A rs886049139
NM_019844.4(SLCO1B3):c.*339G>C rs191491660
NM_019844.4(SLCO1B3):c.*399A>G rs886049141
NM_019844.4(SLCO1B3):c.*437A>G rs1866507319
NM_019844.4(SLCO1B3):c.*560T>C rs886049142
NM_019844.4(SLCO1B3):c.1129T>C (p.Leu377=) rs1474803384
NM_019844.4(SLCO1B3):c.1432G>C (p.Gly478Arg) rs886049137
NM_019844.4(SLCO1B3):c.147A>C (p.Lys49Asn) rs1865106191
NM_019844.4(SLCO1B3):c.1659C>T (p.Thr553=) rs1865736744
NM_019844.4(SLCO1B3):c.1748-12C>T rs886049138
NM_019844.4(SLCO1B3):c.1992A>C (p.Lys664Asn) rs758003128
NM_019844.4(SLCO1B3):c.203dup (p.Leu68fs) rs748195197
NM_019844.4(SLCO1B3):c.291del (p.Ile97fs) rs1565591652
NM_019844.4(SLCO1B3):c.360-3_362del rs772663115
NM_019844.4(SLCO1B3):c.432_435del (p.Asn145fs) rs764867994
NM_019844.4(SLCO1B3):c.518A>G (p.Tyr173Cys) rs886049134
NM_019844.4(SLCO1B3):c.541C>T (p.Arg181Cys) rs746941097
NM_019844.4(SLCO1B3):c.628+4A>T rs886049135
NM_019844.4(SLCO1B3):c.731C>G (p.Thr244Ser) rs1361523872
NM_019844.4(SLCO1B3):c.758G>A (p.Arg253His) rs745538500
NM_019844.4(SLCO1B3):c.803T>G (p.Phe268Cys) rs1449152778
NM_019844.4(SLCO1B3):c.977del (p.Phe326fs) rs769005039

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