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rs188286943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs188286943(C;T)
Make rs188286943(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position46662452
GeneVPS35
is asnp
is mentioned by
dbSNPrs188286943
ebirs188286943
HLIrs188286943
Exacrs188286943
Varsomers188286943
Maprs188286943
PheGenIrs188286943
hapmaprs188286943
1000 genomesrs188286943
hgdprs188286943
ensemblrs188286943
gopubmedrs188286943
geneviewrs188286943
scholarrs188286943
googlers188286943
pharmgkbrs188286943
gwascentralrs188286943
openSNPrs188286943
23andMers188286943
23andMe allrs188286943
SNP Nexus

SNPshotrs188286943
SNPdbers188286943
MSV3drs188286943
GWAS Ctlgrs188286943
Max Magnitude0
ClinVar
Risk rs188286943(T;T)
Alt rs188286943(T;T)
Reference rs188286943(C;C)
Significance Pathogenic
Disease Parkinson disease 17
Variation info
Gene VPS35
CLNDBN Parkinson disease 17
Reversed 0
HGVS NC_000016.9:g.46696364C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023115.5,