ClinVar Miner

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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_019844.4(SLCO1B3):c.727+2087T>C	rs2417940	0.75026
NC_000012.12:g.20921188C>T	rs2117032	0.46485

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