rs2075713
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2075713(G;G) |
| Make rs2075713(G;T) |
| Make rs2075713(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 124748043 |
| Gene | VSIG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075713 |
| dbSNP (classic) | rs2075713 |
| ClinGen | rs2075713 |
| ebi | rs2075713 |
| HLI | rs2075713 |
| Exac | rs2075713 |
| Gnomad | rs2075713 |
| Varsome | rs2075713 |
| LitVar | rs2075713 |
| Map | rs2075713 |
| PheGenI | rs2075713 |
| Biobank | rs2075713 |
| 1000 genomes | rs2075713 |
| hgdp | rs2075713 |
| ensembl | rs2075713 |
| geneview | rs2075713 |
| scholar | rs2075713 |
| rs2075713 | |
| pharmgkb | rs2075713 |
| gwascentral | rs2075713 |
| openSNP | rs2075713 |
| 23andMe | rs2075713 |
| SNPshot | rs2075713 |
| SNPdbe | rs2075713 |
| MSV3d | rs2075713 |
| GWAS Ctlg | rs2075713 |
| GMAF | 0.1942 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 22461181] Functional genetic variation at the NRGN gene and schizophrenia: Evidence from a gene-based case-control study and gene expression analysis
