rs1805477
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(T;T) | 0 | common in clinvar |
Make rs1805477(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 13561795 |
Gene | GRIN2B |
is a | snp |
is | mentioned by |
dbSNP | rs1805477 |
dbSNP (classic) | rs1805477 |
ClinGen | rs1805477 |
ebi | rs1805477 |
HLI | rs1805477 |
Exac | rs1805477 |
Gnomad | rs1805477 |
Varsome | rs1805477 |
LitVar | rs1805477 |
Map | rs1805477 |
PheGenI | rs1805477 |
Biobank | rs1805477 |
1000 genomes | rs1805477 |
hgdp | rs1805477 |
ensembl | rs1805477 |
geneview | rs1805477 |
scholar | rs1805477 |
rs1805477 | |
pharmgkb | rs1805477 |
gwascentral | rs1805477 |
openSNP | rs1805477 |
23andMe | rs1805477 |
SNPshot | rs1805477 |
SNPdbe | rs1805477 |
MSV3d | rs1805477 |
GWAS Ctlg | rs1805477 |
GMAF | 0.07943 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22433450] Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder
ClinVar | |
---|---|
Risk | Rs1805477(C;C) rs1805477(G;G) |
Alt | Rs1805477(C;C) rs1805477(G;G) |
Reference | Rs1805477(T;T) |
Significance | Probable-non-pathogenic |
Disease | Intellectual Disability |
Variation | info |
Gene | GRIN2B |
CLNDBN | Intellectual Disability, Dominant |
Reversed | 0 |
HGVS | NC_000012.11:g.13714729T>C |
CLNSRC | |
CLNACC | RCV000389607.1, |