ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_001365536.1(SCN9A):c.1115G>A (p.Arg372His) rs201071819
NM_001365536.1(SCN9A):c.1604C>T (p.Ser535Leu) rs201354321
NM_001365536.1(SCN9A):c.1675G>A (p.Gly559Ser) rs201569378
NM_001365536.1(SCN9A):c.1714G>A (p.Asp572Asn) rs747040987
NM_001365536.1(SCN9A):c.2085A>G (p.Ile695Met) rs199588089
NM_001365536.1(SCN9A):c.2566A>G (p.Ile856Val) rs1218485798
NM_001365536.1(SCN9A):c.3482G>A (p.Trp1161Ter) rs759003928
NM_001365536.1(SCN9A):c.3599T>A (p.Leu1200His)
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748
NM_001365536.1(SCN9A):c.3944T>C (p.Ile1315Thr) rs202235611
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His) rs79805025

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.