ClinVar Miner

List of variants in gene APOB reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_000384.3(APOB):c.1033G>A (p.Ala345Thr)
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val) rs72654423
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met) rs12713450
NM_000384.3(APOB):c.2302A>G (p.Lys768Glu) rs1553385712
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843
NM_000384.3(APOB):c.5198_5200AAG[1] (p.Glu1734del) rs1553383904
NM_000384.3(APOB):c.751G>A (p.Ala251Thr) rs61741625
NM_000384.3(APOB):c.8661T>C (p.Thr2887=)
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520

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.