rs747838255
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs747838255(A;A) |
Make rs747838255(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 9840746 |
Gene | GRIN2A |
is a | snp |
is | mentioned by |
dbSNP | rs747838255 |
dbSNP (classic) | rs747838255 |
ClinGen | rs747838255 |
ebi | rs747838255 |
HLI | rs747838255 |
Exac | rs747838255 |
Gnomad | rs747838255 |
Varsome | rs747838255 |
LitVar | rs747838255 |
Map | rs747838255 |
PheGenI | rs747838255 |
Biobank | rs747838255 |
1000 genomes | rs747838255 |
hgdp | rs747838255 |
ensembl | rs747838255 |
geneview | rs747838255 |
scholar | rs747838255 |
rs747838255 | |
pharmgkb | rs747838255 |
gwascentral | rs747838255 |
openSNP | rs747838255 |
23andMe | rs747838255 |
SNPshot | rs747838255 |
SNPdbe | rs747838255 |
MSV3d | rs747838255 |
GWAS Ctlg | rs747838255 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747838255(A;A) |
Alt | rs747838255(A;A) |
Reference | Rs747838255(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GRIN2A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.9934603G>A |
CLNSRC | |
CLNACC | RCV000187674.2, |