List of variants in gene APOB reported as benign by Illumina Laboratory Services, Illumina

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: 30

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.7545C>T (p.Thr2515=)	rs693	0.38722
NM_000384.3(APOB):c.2706C>T (p.Asn902=)	rs1801700	0.03627
NM_000384.3(APOB):c.11904-7C>T	rs12720851	0.03622
NM_000384.3(APOB):c.538-9C>T	rs1800478	0.03349
NM_000384.3(APOB):c.10737C>T (p.Thr3579=)	rs12713554	0.02896
NM_000384.3(APOB):c.10701G>A (p.Thr3567=)	rs12713558	0.02176
NM_000384.3(APOB):c.9004C>T (p.Leu3002=)	rs12713600	0.01938
NM_000384.3(APOB):c.4365C>T (p.Phe1455=)	rs12720847	0.01812
NM_000384.3(APOB):c.11808C>T (p.Ile3936=)	rs12720852	0.01624
NM_000384.3(APOB):c.3509-10G>A	rs12720770	0.01624
NM_000384.3(APOB):c.1353-12C>T	rs76202659	0.01423
NM_000384.3(APOB):c.2604+15G>C	rs72653066	0.00842
NM_000384.3(APOB):c.8353A>C (p.Asn2785His)	rs2163204	0.00306
NM_000384.3(APOB):c.1785C>G (p.Ser595=)	rs139864087	0.00247
NM_000384.3(APOB):c.581C>T (p.Thr194Met)	rs13306198	0.00162
NM_000384.3(APOB):c.12581T>C (p.Ile4194Thr)	rs570782024	0.00005
NM_000384.3(APOB):c.5322C>T (p.Tyr1774=)	rs13306188	0.00004
NM_000384.3(APOB):c.7600C>T (p.Arg2534Ter)	rs145143533	0.00001
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln)
NM_000384.3(APOB):c.12809G>C (p.Arg4270Thr)
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val)
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp)
NM_000384.3(APOB):c.1661C>T (p.Pro554Leu)
NM_000384.3(APOB):c.2222C>A (p.Thr741Asn)
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)
NM_000384.3(APOB):c.3201G>A (p.Pro1067=)	rs200281277
NM_000384.3(APOB):c.3634C>A (p.Leu1212Met)
NM_000384.3(APOB):c.433C>T (p.Pro145Ser)
NM_000384.3(APOB):c.9140C>G (p.Thr3047Arg)	rs61742323

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.