ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_002977.3(SCN9A):c.1150G>A (p.Val384Ile) rs200973534
NM_002977.3(SCN9A):c.1966A>G (p.Lys656Glu) rs775090142
NM_002977.3(SCN9A):c.2159T>A (p.Ile720Lys) rs200945460
NM_002977.3(SCN9A):c.2533A>G (p.Ile845Val) rs1218485798
NM_002977.3(SCN9A):c.2611G>C (p.Val871Leu) rs1553487882
NM_002977.3(SCN9A):c.2987G>A (p.Arg996His) rs188145203
NM_002977.3(SCN9A):c.3238A>G (p.Ile1080Val) rs202212176
NM_002977.3(SCN9A):c.3476T>C (p.Ile1159Thr) rs73019664
NM_002977.3(SCN9A):c.3505A>G (p.Asn1169Asp) rs750269576
NM_002977.3(SCN9A):c.3799C>G (p.Leu1267Val) rs180922748
NM_002977.3(SCN9A):c.4115A>G (p.Lys1372Arg) rs779536952
NM_002977.3(SCN9A):c.4228-3T>C rs773953311
NM_002977.3(SCN9A):c.4997A>T (p.Asp1666Val) rs1553473210
NM_002977.3(SCN9A):c.5678G>A (p.Arg1893His) rs79805025
NM_002977.3(SCN9A):c.5758G>C (p.Asp1920His) rs200410805

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.