rs147455037
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs147455037(C;T) |
Make rs147455037(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 38113560 |
Gene | PLA2G6 |
is a | snp |
is | mentioned by |
dbSNP | rs147455037 |
dbSNP (classic) | rs147455037 |
ClinGen | rs147455037 |
ebi | rs147455037 |
HLI | rs147455037 |
Exac | rs147455037 |
Gnomad | rs147455037 |
Varsome | rs147455037 |
LitVar | rs147455037 |
Map | rs147455037 |
PheGenI | rs147455037 |
Biobank | rs147455037 |
1000 genomes | rs147455037 |
hgdp | rs147455037 |
ensembl | rs147455037 |
geneview | rs147455037 |
scholar | rs147455037 |
rs147455037 | |
pharmgkb | rs147455037 |
gwascentral | rs147455037 |
openSNP | rs147455037 |
23andMe | rs147455037 |
SNPshot | rs147455037 |
SNPdbe | rs147455037 |
MSV3d | rs147455037 |
GWAS Ctlg | rs147455037 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147455037(T;T) |
Alt | rs147455037(T;T) |
Reference | Rs147455037(C;C) |
Significance | Probable-Pathogenic |
Disease | Abnormality of brain morphology |
Variation | info |
Gene | PLA2G6 |
CLNDBN | Abnormality of brain morphology |
Reversed | 0 |
HGVS | NC_000022.10:g.38509567C>T |
CLNSRC | |
CLNACC | RCV000454205.1, |