{{Rsnum
|rsid=41268673
|Gene=SCN9A
|Chromosome=2
|position=166284599
|Orientation=plus
|GMAF=0.01561
|Gene_s=SCN9A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=41268673
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=167141109
|CHROM=2
|GMAF=0.0156
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050168000000140516110100
|GENEINFO=SCN9A:6335
|GENE_NAME=SCN9A
|GENE_ID=6335
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.167141109G>T
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=133020
|CLNDBN=Primary erythromelalgia
|Tags=PM;PMC;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9844; 0.01561
|CLNACC=RCV000020511.3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1163:C0014805:133020:306577:90026:403390002
|CLNSRC=GeneReviews
|CLNSRCID=NBK1163
|COMMON=1
|Disease=Primary erythromelalgia
}}

{{PMID Auto
|PMID=15955112
|Title=SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.
}}

{{GET Evidence
|gene=SCN9A
|aa_change=Pro610Thr
|aa_change_short=P610T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs41268673
|overall_frequency_n=210
|overall_frequency_d=10628
|overall_frequency=0.0197591
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=2
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|pph2_score=0.005
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=4
|autoscore=3
|n_web_uneval=9
}}

{{PMID Auto
|PMID=23129781
|Title=Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}