List of variants in gene combination SLCO1B3, SLCO1B3-SLCO1B7 reported as pathogenic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_019844.4(SLCO1B3):c.971-2A>G	rs140033394	0.00012
NM_019844.4(SLCO1B3):c.1135+1G>A	rs201833947	0.00006
NM_019844.4(SLCO1B3):c.1747+1G>A	rs373707046	0.00001
NM_019844.4(SLCO1B3):c.1637dup (p.Leu546fs)	rs78627909
NM_019844.4(SLCO1B3):c.205_209dup (p.Asp70fs)	rs558592800

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