{{Rsnum
|rsid=121908910
|Gene=SCN9A
|Chromosome=2
|position=166272731
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=AC010127.3,SCN9A
}}{{omim
|id=603415
|rsnum=121908910
|variant=0008
}}{{ClinVar
|rsid=121908910
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=167129241
|CHROM=2
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=SCN9A:6335
|GENE_NAME=SCN9A
|GENE_ID=6335
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.167129241G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603415.0008
|CLNSIG=5
|CLNCUI=C1833661
|CLNDBN=Paroxysmal extreme pain disorder
|Disease=Paroxysmal extreme pain disorder
|CLNACC=RCV000006728.1
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833661:167400:46348
|COMMON=0
}}