{{Rsnum
|rsid=28937592
|Gene=SNCAIP
|Chromosome=5
|position=122450708
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.001377
|Gene_s=MGC32805,SNCAIP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|desc=PARKINSON DISEASE
|id=603779
|rsnum=28937592
|variant=0001
}}

{{ClinVar
|rsid=28937592
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=121786403
|CHROM=5
|GMAF=0.0014
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000040416110100
|GENEINFO=SNCAIP:9627; MGC32805:153163
|GENE_NAME=SNCAIP; MGC32805
|GENE_ID=9627; 153163
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.121786403C>T
|CLNORIGIN=1
|Tags=PM;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNACC=RCV000006451.1
|CLNDBN=Reclassified - variant of unknown significance
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603779.0001
|COMMON=0
|Disease=Reclassified - variant of unknown significance
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}