ClinVar Miner

List of variants studied for Parietal foramina 2 by Genome-Nilou Lab

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_021926.4(ALX4):c.621A>G (p.Ser207=) rs10769028 0.99242
NM_021926.4(ALX4):c.467-45T>C rs11037929 0.95917
NM_021926.4(ALX4):c.778-117T>C rs10742699 0.79676
NM_021926.4(ALX4):c.778-140G>C rs10769024 0.57195
NM_021926.4(ALX4):c.104G>C (p.Arg35Thr) rs3824915 0.42227
NM_021926.4(ALX4):c.304C>T (p.Pro102Ser) rs12421995 0.32933
NM_021926.4(ALX4):c.1074C>T (p.His358=) rs3802805 0.29957
NM_021926.4(ALX4):c.778-11G>A rs75147697 0.08417

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.