rs199935023
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs199935023(A;A) |
Make rs199935023(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 38132917 |
Gene | PLA2G6 |
is a | snp |
is | mentioned by |
dbSNP | rs199935023 |
dbSNP (classic) | rs199935023 |
ClinGen | rs199935023 |
ebi | rs199935023 |
HLI | rs199935023 |
Exac | rs199935023 |
Gnomad | rs199935023 |
Varsome | rs199935023 |
LitVar | rs199935023 |
Map | rs199935023 |
PheGenI | rs199935023 |
Biobank | rs199935023 |
1000 genomes | rs199935023 |
hgdp | rs199935023 |
ensembl | rs199935023 |
geneview | rs199935023 |
scholar | rs199935023 |
rs199935023 | |
pharmgkb | rs199935023 |
gwascentral | rs199935023 |
openSNP | rs199935023 |
23andMe | rs199935023 |
SNPshot | rs199935023 |
SNPdbe | rs199935023 |
MSV3d | rs199935023 |
GWAS Ctlg | rs199935023 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199935023(A;A) rs199935023(T;T) |
Alt | rs199935023(A;A) rs199935023(T;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, |