rs1126442
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1126442(A;A) |
Make rs1126442(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 137156924 |
Gene | GRIN1, LOC105376328 |
is a | snp |
is | mentioned by |
dbSNP | rs1126442 |
dbSNP (classic) | rs1126442 |
ClinGen | rs1126442 |
ebi | rs1126442 |
HLI | rs1126442 |
Exac | rs1126442 |
Gnomad | rs1126442 |
Varsome | rs1126442 |
LitVar | rs1126442 |
Map | rs1126442 |
PheGenI | rs1126442 |
Biobank | rs1126442 |
1000 genomes | rs1126442 |
hgdp | rs1126442 |
ensembl | rs1126442 |
geneview | rs1126442 |
scholar | rs1126442 |
rs1126442 | |
pharmgkb | rs1126442 |
gwascentral | rs1126442 |
openSNP | rs1126442 |
23andMe | rs1126442 |
SNPshot | rs1126442 |
SNPdbe | rs1126442 |
MSV3d | rs1126442 |
GWAS Ctlg | rs1126442 |
GMAF | 0.1616 |
Max Magnitude | 0 |
[PMID 23880023] Genetic variation of GRIN1 confers vulnerability to methamphetamine-dependent psychosis in a Thai population
ClinVar | |
---|---|
Risk | rs1126442(A;A) |
Alt | rs1126442(A;A) |
Reference | Rs1126442(G;G) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | GRIN1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000009.11:g.140051376G>A |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000117172.3, |