{{Rsnum
|rsid=267607087
|Chromosome=9
|position=92047261
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SPTLC1
|Gene_s=SPTLC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=A
|CHROM=9
|CLNACC=RCV000005071.1
|CLNALLE=1
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE
|CLNDSDB=MedGen
|CLNDSDBID=CN068845
|CLNHGVS=NC_000009.11:g.94809543G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605712.0005
|Disease=NEUROPATHY
|FwdALT=T
|FwdREF=C
|GENEINFO=SPTLC1:10558
|GENE_ID=10558
|GENE_NAME=SPTLC1
|REF=G
|RSPOS=94809543
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607087
}}