{{Rsnum
|rsid=104894393
|Chromosome=13
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FGF14
|position=101726785
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGF14
}}{{omim
|id=601515
|rsnum=104894393
|variant=0001
}}{{ClinVar
|rsid=104894393
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=102379135
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGF14:2259
|GENE_NAME=FGF14
|GENE_ID=2259
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.102379135A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601515.0001
|CLNSIG=5
|CLNCUI=C1836383
|CLNDBN=Spinocerebellar ataxia 27
|Disease=Spinocerebellar ataxia 27
|CLNACC=RCV000008584.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1836383:609307:98764
}}