rs776061422
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs776061422(A;A) |
Make rs776061422(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 6254689 |
Gene | GPR153 |
is a | snp |
is | mentioned by |
dbSNP | rs776061422 |
dbSNP (classic) | rs776061422 |
ClinGen | rs776061422 |
ebi | rs776061422 |
HLI | rs776061422 |
Exac | rs776061422 |
Gnomad | rs776061422 |
Varsome | rs776061422 |
LitVar | rs776061422 |
Map | rs776061422 |
PheGenI | rs776061422 |
Biobank | rs776061422 |
1000 genomes | rs776061422 |
hgdp | rs776061422 |
ensembl | rs776061422 |
geneview | rs776061422 |
scholar | rs776061422 |
rs776061422 | |
pharmgkb | rs776061422 |
gwascentral | rs776061422 |
openSNP | rs776061422 |
23andMe | rs776061422 |
SNPshot | rs776061422 |
SNPdbe | rs776061422 |
MSV3d | rs776061422 |
GWAS Ctlg | rs776061422 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776061422(A;A) |
Alt | rs776061422(A;A) |
Reference | Rs776061422(G;G) |
Significance | Probable-Pathogenic |
Disease | Childhood-Onset Schizophrenia |
Variation | info |
Gene | GPR153 |
CLNDBN | Childhood-Onset Schizophrenia |
Reversed | 0 |
HGVS | NC_000001.10:g.6314749G>A |
CLNSRC | |
CLNACC | RCV000202336.1, |