ClinVar Miner

List of variants in gene CHRNA4 reported as uncertain significance for Seizures

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_000744.6(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652
NM_000744.6(CHRNA4):c.1138A>G (p.Ser380Gly) rs187372416
NM_000744.6(CHRNA4):c.1144C>T (p.Pro382Ser) rs1568809115
NM_000744.6(CHRNA4):c.1228G>A (p.Val410Ile) rs121912272
NM_000744.6(CHRNA4):c.1273C>T (p.Pro425Ser) rs764808511
NM_000744.6(CHRNA4):c.1454G>A (p.Arg485Gln) rs755416498
NM_000744.6(CHRNA4):c.1525G>A (p.Ala509Thr) rs142137599
NM_000744.6(CHRNA4):c.1721T>C (p.Ile574Thr) rs139657121
NM_000744.6(CHRNA4):c.200G>A (p.Gly67Asp) rs1568819500
NM_000744.6(CHRNA4):c.622G>A (p.Glu208Lys) rs771249249
NM_000744.6(CHRNA4):c.971C>T (p.Thr324Met) rs531615515

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.