{{Rsnum
|rsid=104893878
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SNCA
|position=89835580
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FGF22,SNCA
}}{{omim
|id=163890
|rsnum=104893878
|variant=0002
}}{{ClinVar
|rsid=104893878
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=90756731
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SNCA:6622; RP11-67M1.1:644248
|GENE_NAME=SNCA; RP11-67M1.1
|GENE_ID=6622; 644248
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.90756731C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000015045.25
|CLNDBN=Parkinson disease 1, autosomal dominant
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=163890.0002
|Disease=Parkinson disease 1
}}