Have questions? Visit https://www.reddit.com/r/SNPedia

rs397514694

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514694(G;T)
Make rs397514694(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position161350205
GenePARK2
is asnp
is mentioned by
dbSNPrs397514694
ebirs397514694
HLIrs397514694
Exacrs397514694
Varsomers397514694
Maprs397514694
PheGenIrs397514694
hapmaprs397514694
1000 genomesrs397514694
hgdprs397514694
ensemblrs397514694
gopubmedrs397514694
geneviewrs397514694
scholarrs397514694
googlers397514694
pharmgkbrs397514694
gwascentralrs397514694
openSNPrs397514694
23andMers397514694
23andMe allrs397514694
SNP Nexus

SNPshotrs397514694
SNPdbers397514694
MSV3drs397514694
GWAS Ctlgrs397514694
Max Magnitude0
ClinVar
Risk rs397514694(T;T)
Alt rs397514694(T;T)
Reference rs397514694(G;G)
Significance Pathogenic
Disease Parkinson disease 2
Variation info
Gene PARK2
CLNDBN Parkinson disease 2
Reversed 1
HGVS NC_000006.11:g.161771237C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043509.3,