ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance for Hereditary sensory and autonomic neuropathy type IIA

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
NM_001365536.1(SCN9A):c.2129G>A (p.Cys710Tyr) rs201709980
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126
NM_001365536.1(SCN9A):c.2299C>T (p.Pro767Ser)
NM_001365536.1(SCN9A):c.3349G>T (p.Val1117Leu) rs200817435
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327
NM_001365536.1(SCN9A):c.4243G>A (p.Ala1415Thr)
NM_001365536.1(SCN9A):c.5588T>C (p.Met1863Thr)

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.