rs2267369
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2267369(C;T) |
Make rs2267369(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 38169340 |
Gene | PLA2G6 |
is a | snp |
is | mentioned by |
dbSNP | rs2267369 |
dbSNP (classic) | rs2267369 |
ClinGen | rs2267369 |
ebi | rs2267369 |
HLI | rs2267369 |
Exac | rs2267369 |
Gnomad | rs2267369 |
Varsome | rs2267369 |
LitVar | rs2267369 |
Map | rs2267369 |
PheGenI | rs2267369 |
Biobank | rs2267369 |
1000 genomes | rs2267369 |
hgdp | rs2267369 |
ensembl | rs2267369 |
geneview | rs2267369 |
scholar | rs2267369 |
rs2267369 | |
pharmgkb | rs2267369 |
gwascentral | rs2267369 |
openSNP | rs2267369 |
23andMe | rs2267369 |
SNPshot | rs2267369 |
SNPdbe | rs2267369 |
MSV3d | rs2267369 |
GWAS Ctlg | rs2267369 |
GMAF | 0.0753 |
Max Magnitude | 0 |
? | (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, |