{{Rsnum
|rsid=121908918
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SCN9A
|position=166284506
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AC010127.3,SCN9A
}}{{omim
|id=603415
|rsnum=121908918
|variant=0018
}}{{ClinVar
|rsid=121908918
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=167141016
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN9A:6335
|GENE_NAME=SCN9A
|GENE_ID=6335
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.167141016T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603415.0018
|CLNSIG=5
|CLNCUI=C2751777
|CLNDBN=Generalized epilepsy with febrile seizures plus, type 7
|Disease=Generalized epilepsy with febrile seizures plus
|CLNACC=RCV000006738.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751777:613863:36387
}}