ClinVar Miner

List of variants in gene combination SLCO1B3, SLCO1B3-SLCO1B7 reported as likely benign for bilirubin metabolism disease

Included ClinVar conditions (39):
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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_019844.4(SLCO1B3):c.439A>G (p.Thr147Ala) rs57585902 0.00971
NM_019844.4(SLCO1B3):c.1679T>C (p.Val560Ala) rs12299012 0.00802
NM_019844.4(SLCO1B3):c.11A>G (p.His4Arg) rs61612406 0.00698
NM_019844.4(SLCO1B3):c.108C>G (p.Phe36Leu) rs79042365 0.00606
NM_019844.4(SLCO1B3):c.1347A>G (p.Ala449=) rs79382866 0.00482
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.1614T>C (p.Val538=) rs77851390 0.00265
NM_019844.4(SLCO1B3):c.1593A>G (p.Thr531=) rs142694767 0.00060
NM_019844.4(SLCO1B3):c.1857A>T (p.Val619=) rs143827641 0.00051
NM_019844.4(SLCO1B3):c.727+7A>G rs376199890 0.00046
NM_019844.4(SLCO1B3):c.459A>G (p.Thr153=) rs370334648 0.00008
NM_019844.4(SLCO1B3):c.264A>C (p.Gly88=) rs374616195 0.00002
NM_019844.4(SLCO1B3):c.1241C>T (p.Thr414Ile) rs146940490
NM_019844.4(SLCO1B3):c.1464A>G (p.Gly488=)
NM_019844.4(SLCO1B3):c.1974A>C (p.Ala658=) rs774423704
NM_019844.4(SLCO1B3):c.481+12_481+25del rs766220111
NM_019844.4(SLCO1B3):c.481+3A>G rs199631489
NM_019844.4(SLCO1B3):c.481+7A>G

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