{{Rsnum
|rsid=80338762
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SEPT9
|position=77402314
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SEPT9
}}{{omim
|id=604061
|rsnum=80338762
|variant=0002
}}{{ClinVar
|rsid=80338762
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=75398396
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SEPT9:10801
|GENE_NAME=SEPT9
|GENE_ID=10801
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.75398396C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1395; 604061.0002
|CLNSIG=5
|CLNCUI=C1834304; C1834304
|CLNDBN=Hereditary neuralgic amyotrophy
|Disease=Hereditary neuralgic amyotrophy
|CLNACC=RCV000006222.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1395:C1834304:162100:2901
}}{{PMID Auto
|PMID=16186812
|Title=Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
}}