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rs2267369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2267369(C;T)
Make rs2267369(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position38169340
GenePLA2G6
is asnp
is mentioned by
dbSNPrs2267369
dbSNP (classic)rs2267369
ClinGenrs2267369
ebirs2267369
HLIrs2267369
Exacrs2267369
Gnomadrs2267369
Varsomers2267369
LitVarrs2267369
Maprs2267369
PheGenIrs2267369
Biobankrs2267369
1000 genomesrs2267369
hgdprs2267369
ensemblrs2267369
geneviewrs2267369
scholarrs2267369
googlers2267369
pharmgkbrs2267369
gwascentralrs2267369
openSNPrs2267369
23andMers2267369
SNPshotrs2267369
SNPdbers2267369
MSV3drs2267369
GWAS Ctlgrs2267369
GMAF0.0753
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22459563] Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population


ClinVar
Risk rs2267369(T;T)
Alt rs2267369(T;T)
Reference Rs2267369(C;C)
Significance Probable-non-pathogenic
Disease not specified Infantile neuroaxonal dystrophy
Variation info
Gene PLA2G6
CLNDBN not specified Infantile neuroaxonal dystrophy
Reversed 0
HGVS NC_000022.10:g.38565347C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000147337.1, RCV000299100.1,