ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_000384.2(APOB):c.10556C>T (p.Thr3519Ile) rs746951119
NM_000384.2(APOB):c.10672C>T (p.Arg3558Cys) rs12713559
NM_000384.2(APOB):c.10708C>T (p.His3570Tyr) rs201736972
NM_000384.2(APOB):c.11761G>A (p.Val3921Ile) rs72654409
NM_000384.2(APOB):c.13154G>A (p.Arg4385His) rs533755016
NM_000384.2(APOB):c.13181T>C (p.Val4394Ala) rs12720843
NM_000384.2(APOB):c.13288T>A (p.Ser4430Thr) rs72654426
NM_000384.2(APOB):c.2914G>A (p.Gly972Ser) rs199893862
NM_000384.2(APOB):c.2981C>T (p.Pro994Leu) rs41288783
NM_000384.2(APOB):c.3427C>T (p.Pro1143Ser) rs72653077
NM_000384.2(APOB):c.5066G>A (p.Arg1689His) rs151009667
NM_000384.2(APOB):c.5599C>T (p.Arg1867Trp) rs200583769
NM_000384.2(APOB):c.6655C>T (p.Arg2219Cys) rs141641980
NM_000384.2(APOB):c.7285T>A (p.Ser2429Thr) rs72653092
NM_000384.2(APOB):c.7698G>C (p.Glu2566Asp) rs149306841
NM_000384.2(APOB):c.7853T>C (p.Ile2618Thr) rs531273434
NM_000384.2(APOB):c.8550T>G (p.Ile2850Met) rs148498577
NM_000384.2(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.