rs876661064
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876661064(C;T) |
Make rs876661064(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 12 |
Position | 13569988 |
Gene | GRIN2B |
is a | snp |
is | mentioned by |
dbSNP | rs876661064 |
dbSNP (classic) | rs876661064 |
ClinGen | rs876661064 |
ebi | rs876661064 |
HLI | rs876661064 |
Exac | rs876661064 |
Gnomad | rs876661064 |
Varsome | rs876661064 |
LitVar | rs876661064 |
Map | rs876661064 |
PheGenI | rs876661064 |
Biobank | rs876661064 |
1000 genomes | rs876661064 |
hgdp | rs876661064 |
ensembl | rs876661064 |
geneview | rs876661064 |
scholar | rs876661064 |
rs876661064 | |
pharmgkb | rs876661064 |
gwascentral | rs876661064 |
openSNP | rs876661064 |
23andMe | rs876661064 |
SNPshot | rs876661064 |
SNPdbe | rs876661064 |
MSV3d | rs876661064 |
GWAS Ctlg | rs876661064 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661064(T;T) |
Alt | rs876661064(T;T) |
Reference | Rs876661064(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GRIN2B |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.13722922G>A |
CLNSRC | |
CLNACC | RCV000222391.1, |