{{Rsnum
|rsid=104893668
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ST3GAL5
|position=85844542
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ST3GAL5
}}{{omim
|id=604402
|rsnum=104893668
|variant=0001
}}{{ClinVar
|rsid=104893668
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=86071665
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=ST3GAL5:8869
|GENE_NAME=ST3GAL5
|GENE_ID=8869
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.86071665G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604402.0001
|CLNSIG=5
|CLNCUI=C1836824
|CLNDBN=Amish infantile epilepsy syndrome
|Disease=Amish infantile epilepsy syndrome
|CLNACC=RCV000005895.2
|Tags=RV;PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836824:609056:171714
}}