{{Rsnum
|rsid=80356468
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN9A
|position=166306571
|Gene_s=SCN9A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356468
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=167163081
|CHROM=2
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SCN9A:6335
|GENE_NAME=SCN9A
|GENE_ID=6335
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.167163081T>C
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=133020
|CLNDBN=Primary erythromelalgia
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000020515.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1163:C0014805:133020:306577:90026:403390002
|CLNSRC=GeneReviews
|CLNSRCID=NBK1163
|Disease=Primary erythromelalgia
}}{{PMID Auto
|PMID=17294067
|Title=Characterization of a familial case with primary erythromelalgia from Taiwan.
}}

{{PMID Auto
|PMID=18171466
|Title=Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade.
|OA=1
}}