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rs387906863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906863(A;A)
Make rs387906863(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position38115657
GenePLA2G6
is asnp
is mentioned by
dbSNPrs387906863
ebirs387906863
HLIrs387906863
Exacrs387906863
Varsomers387906863
Maprs387906863
PheGenIrs387906863
hapmaprs387906863
1000 genomesrs387906863
hgdprs387906863
ensemblrs387906863
gopubmedrs387906863
geneviewrs387906863
scholarrs387906863
googlers387906863
pharmgkbrs387906863
gwascentralrs387906863
openSNPrs387906863
23andMers387906863
23andMe allrs387906863
SNP Nexus

SNPshotrs387906863
SNPdbers387906863
MSV3drs387906863
GWAS Ctlgrs387906863
Max Magnitude0
ClinVar
Risk rs387906863(A,T;A,T)
Alt rs387906863(A,T;A,T)
Reference rs387906863(G;G)
Significance Pathogenic
Disease Parkinson disease 14
Variation info
Gene PLA2G6
CLNDBN Parkinson disease 14
Reversed 1
HGVS NC_000022.10:g.38511664C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023314.4,