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rs387906864

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906864(C;T)
Make rs387906864(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position38126444
GenePLA2G6
is asnp
is mentioned by
dbSNPrs387906864
ebirs387906864
HLIrs387906864
Exacrs387906864
Varsomers387906864
Maprs387906864
PheGenIrs387906864
hapmaprs387906864
1000 genomesrs387906864
hgdprs387906864
ensemblrs387906864
gopubmedrs387906864
geneviewrs387906864
scholarrs387906864
googlers387906864
pharmgkbrs387906864
gwascentralrs387906864
openSNPrs387906864
23andMers387906864
23andMe allrs387906864
SNP Nexus

SNPshotrs387906864
SNPdbers387906864
MSV3drs387906864
GWAS Ctlgrs387906864
Max Magnitude0
ClinVar
Risk rs387906864(T;T)
Alt rs387906864(T;T)
Reference rs387906864(C;C)
Significance Pathogenic
Disease Parkinson disease 14
Variation info
Gene PLA2G6
CLNDBN Parkinson disease 14
Reversed 1
HGVS NC_000022.10:g.38522451G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023315.3,