ClinVar Miner

List of variants in gene ATM reported as likely benign by University of Washington Department of Laboratory Medicine,University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_000051.3(ATM):c.-31+1129T>A rs552689366
NM_000051.3(ATM):c.-31+1135C>T rs869312481
NM_000051.3(ATM):c.-31+1782A>C rs749439725
NM_000051.3(ATM):c.185+616T>C rs4987905
NM_000051.3(ATM):c.2124+409A>G rs869312477
NM_000051.3(ATM):c.2125-88T>A rs189045169
NM_000051.3(ATM):c.2377-397A>G rs869312476
NM_000051.3(ATM):c.2838+1131C>T rs11212574
NM_000051.3(ATM):c.2838+194A>G rs749105426
NM_000051.3(ATM):c.3284+382T>C rs189826589
NM_000051.3(ATM):c.3747-34A>G rs3092840
NM_000051.3(ATM):c.3993+133A>G rs142220799
NM_000051.3(ATM):c.3994-830A>C rs869312479
NM_000051.3(ATM):c.4109+54A>T rs181020146
NM_000051.3(ATM):c.5005+302A>T rs869312480
NM_000051.3(ATM):c.5320-23T>A rs753483198
NM_000051.3(ATM):c.5496+231G>A rs4988039

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.