{{Rsnum
|rsid=28941770
|Gene=HEXA
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=15
|position=72353105
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HEXA
}}{{omim
|desc=[[Tay-Sachs disease]]
|id=606869
|rsnum=28941770
|variant=0024
}}
{{ neighbor
| rsid = 28941771
| distance = 5
}}

{{omim
|id=606869
|rsnum=28941770
|variant=0006
}}

{{ClinVar
|rsid=28941770
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=72645446
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HEXA:3073
|GENE_NAME=HEXA
|GENE_ID=3073
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000015.9:g.72645446C>A; NC_000015.9:g.72645446C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606869.0024; 606869.0006
|CLNSIG=5
|CLNCUI=C0039373; CN068770
|CLNDBN=Tay-Sachs disease; Tay-sachs disease, b1 variant; Hexa, dn allele
|Disease=Tay-Sachs disease; Tay-sachs disease; Hexa
|CLNACC=RCV000004118.1; RCV000004100.1; RCV000004101.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1218:C0039373:272800:845:111385000; CN068770
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}