rs1042113
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1042113(A;A) |
| Make rs1042113(A;G) |
| Make rs1042113(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 35286822 |
| Gene | SLC1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1042113 |
| dbSNP (classic) | rs1042113 |
| ClinGen | rs1042113 |
| ebi | rs1042113 |
| HLI | rs1042113 |
| Exac | rs1042113 |
| Gnomad | rs1042113 |
| Varsome | rs1042113 |
| LitVar | rs1042113 |
| Map | rs1042113 |
| PheGenI | rs1042113 |
| Biobank | rs1042113 |
| 1000 genomes | rs1042113 |
| hgdp | rs1042113 |
| ensembl | rs1042113 |
| geneview | rs1042113 |
| scholar | rs1042113 |
| rs1042113 | |
| pharmgkb | rs1042113 |
| gwascentral | rs1042113 |
| openSNP | rs1042113 |
| 23andMe | rs1042113 |
| SNPshot | rs1042113 |
| SNPdbe | rs1042113 |
| MSV3d | rs1042113 |
| GWAS Ctlg | rs1042113 |
| GMAF | 0.2691 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Association study of polymorphisms in the excitatory amino acid transporter 2 gene (SLC1A2) with schizophrenia.[PMID 15296513
]
Usefulness of direct sequencing of pooled DNA for SNP identification and allele-frequency determination compatible with a common disease/common variant hypothesis.[PMID 20449810]
Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.[PMID 18852346]
