{{Rsnum
|rsid=121907986
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HEXB
|position=74713584
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HEXB
}}{{omim
|id=606873
|rsnum=121907986
|variant=0017
}}{{ClinVar
|rsid=121907986
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=74009409
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HEXB:3074
|GENE_NAME=HEXB
|GENE_ID=3074
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.74009409C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606873.0017
|CLNSIG=5
|CLNCUI=C0751490
|CLNDBN=Sandhoff disease, infantile
|Disease=Sandhoff disease
|CLNACC=RCV000004091.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C0751490
}}