rs876661041
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs876661041(A;G) |
| Make rs876661041(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 12 |
| Position | 13608643 |
| Gene | GRIN2B, LOC105369668 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876661041 |
| dbSNP (classic) | rs876661041 |
| ClinGen | rs876661041 |
| ebi | rs876661041 |
| HLI | rs876661041 |
| Exac | rs876661041 |
| Gnomad | rs876661041 |
| Varsome | rs876661041 |
| LitVar | rs876661041 |
| Map | rs876661041 |
| PheGenI | rs876661041 |
| Biobank | rs876661041 |
| 1000 genomes | rs876661041 |
| hgdp | rs876661041 |
| ensembl | rs876661041 |
| geneview | rs876661041 |
| scholar | rs876661041 |
| rs876661041 | |
| pharmgkb | rs876661041 |
| gwascentral | rs876661041 |
| openSNP | rs876661041 |
| 23andMe | rs876661041 |
| SNPshot | rs876661041 |
| SNPdbe | rs876661041 |
| MSV3d | rs876661041 |
| GWAS Ctlg | rs876661041 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs876661041(G;G) |
| Alt | rs876661041(G;G) |
| Reference | Rs876661041(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GRIN2B |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000012.11:g.13761577T>C |
| CLNSRC | |
| CLNACC | RCV000215266.1, |
