ClinVar Miner

List of variants in gene NODAL reported as likely benign for Holoprosencephaly sequence

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_018055.5(NODAL):c.*677C>T rs184218697
NM_018055.5(NODAL):c.281G>A (p.Arg94Gln) rs146018217
NM_018055.5(NODAL):c.417C>T (p.Val139=) rs764201898
NM_018055.5(NODAL):c.607G>A (p.Glu203Lys) rs10999334
NM_018055.5(NODAL):c.904C>T (p.Arg302Cys) rs150819707
NM_018055.5(NODAL):c.963G>A (p.Leu321=) rs772060498

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.