{{Rsnum
|rsid=267607091
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SPTLC2
|position=77518097
|Gene_s=SPTLC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=14
|CLNACC=RCV000005066.1
|CLNALLE=1
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE
|CLNDSDB=MedGen
|CLNDSDBID=CN068844
|CLNHGVS=NC_000014.8:g.77984440T>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605713.0003
|Disease=NEUROPATHY
|FwdALT=T
|FwdREF=A
|GENEINFO=SPTLC2:9517
|GENE_ID=9517
|GENE_NAME=SPTLC2
|REF=T
|RSPOS=77984440
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607091
}}