{{Rsnum
|rsid=267607090
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SPTLC2
|position=77555401
|Gene_s=SPTLC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=14
|CLNACC=RCV000005065.1
|CLNALLE=1
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY, TYPE IC
|CLNDSDB=MedGen
|CLNDSDBID=CN068843
|CLNHGVS=NC_000014.8:g.78021744C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605713.0002
|Disease=NEUROPATHY
|FwdALT=A
|FwdREF=G
|GENEINFO=SPTLC2:9517
|GENE_ID=9517
|GENE_NAME=SPTLC2
|REF=C
|RSPOS=78021744
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607090
}}