List of variants in gene combination SLCO1B3, SLCO1B3-SLCO1B7 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_019844.4(SLCO1B3):c.1679T>C (p.Val560Ala)	rs12299012	0.00802
NM_019844.4(SLCO1B3):c.275A>G (p.His92Arg)	rs144099822	0.00250
NM_019844.4(SLCO1B3):c.154A>G (p.Ile52Val)	rs57325543	0.00242
NM_019844.4(SLCO1B3):c.434A>G (p.Asn145Ser)	rs146623116	0.00184
NM_019844.4(SLCO1B3):c.335C>A (p.Ser112Tyr)	rs145334570	0.00052
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.1610A>G (p.Tyr537Cys)	rs150998576	0.00034
NM_019844.4(SLCO1B3):c.1712C>G (p.Ala571Gly)	rs76963574	0.00034
NM_019844.4(SLCO1B3):c.1309G>A (p.Gly437Ser)	rs61673910	0.00031
NM_019844.4(SLCO1B3):c.484T>G (p.Cys162Gly)	rs140353351	0.00021
NM_019844.4(SLCO1B3):c.1794_1795del (p.Cys599fs)	rs766686725	0.00017
NM_019844.4(SLCO1B3):c.1313T>C (p.Leu438Pro)	rs189943255	0.00016
NM_019844.4(SLCO1B3):c.404C>T (p.Ser135Leu)	rs150039066	0.00013
NM_019844.4(SLCO1B3):c.560C>G (p.Pro187Arg)	rs368572652	0.00008
NM_019844.4(SLCO1B3):c.1598A>G (p.Lys533Arg)	rs751785190	0.00003
NM_019844.4(SLCO1B3):c.227G>T (p.Gly76Val)	rs368091191	0.00003
NM_019844.4(SLCO1B3):c.683C>A (p.Ser228Tyr)	rs760497665	0.00001
NM_019844.4(SLCO1B3):c.1200C>A (p.Phe400Leu)
NM_019844.4(SLCO1B3):c.1732G>C (p.Val578Leu)
NM_019844.4(SLCO1B3):c.1843A>G (p.Ile615Val)
NM_019844.4(SLCO1B3):c.263G>T (p.Gly88Val)
NM_019844.4(SLCO1B3):c.67C>T (p.Arg23Cys)
NM_019844.4(SLCO1B3):c.728-4C>G	rs759435706

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.