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rs199935023

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199935023(A;A)
Make rs199935023(A;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position38132917
GenePLA2G6
is asnp
is mentioned by
dbSNPrs199935023
ebirs199935023
HLIrs199935023
Exacrs199935023
Varsomers199935023
Maprs199935023
PheGenIrs199935023
hapmaprs199935023
1000 genomesrs199935023
hgdprs199935023
ensemblrs199935023
gopubmedrs199935023
geneviewrs199935023
scholarrs199935023
googlers199935023
pharmgkbrs199935023
gwascentralrs199935023
openSNPrs199935023
23andMers199935023
23andMe allrs199935023
SNP Nexus

SNPshotrs199935023
SNPdbers199935023
MSV3drs199935023
GWAS Ctlgrs199935023
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs199935023(A,T;A,T)
Alt rs199935023(A,T;A,T)
Reference rs199935023(C;C)
Significance Pathogenic
Disease Parkinson disease 14
Variation info
Gene PLA2G6
CLNDBN Parkinson disease 14
Reversed 0
HGVS NC_000022.10:g.38528924C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023319.4,