ClinVar Miner

List of variants in gene APC reported as uncertain significance by True Health Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_000038.6(APC):c.1631T>C (p.Ile544Thr) rs144056494
NM_000038.6(APC):c.2444A>C (p.Asn815Thr) rs762990578
NM_000038.6(APC):c.2719G>A (p.Gly907Arg) rs771458366
NM_000038.6(APC):c.449A>G (p.Lys150Arg) rs371085910
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr) rs372305287
NM_000038.6(APC):c.775C>T (p.Arg259Trp) rs762117133
NM_000038.6(APC):c.8038C>T (p.Pro2680Ser) rs587780553

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.