rs677221
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs677221(C;C) |
| Make rs677221(C;G) |
| Make rs677221(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 82554641 |
| Gene | NRG3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs677221 |
| dbSNP (classic) | rs677221 |
| ClinGen | rs677221 |
| ebi | rs677221 |
| HLI | rs677221 |
| Exac | rs677221 |
| Gnomad | rs677221 |
| Varsome | rs677221 |
| LitVar | rs677221 |
| Map | rs677221 |
| PheGenI | rs677221 |
| Biobank | rs677221 |
| 1000 genomes | rs677221 |
| hgdp | rs677221 |
| ensembl | rs677221 |
| geneview | rs677221 |
| scholar | rs677221 |
| rs677221 | |
| pharmgkb | rs677221 |
| gwascentral | rs677221 |
| openSNP | rs677221 |
| 23andMe | rs677221 |
| SNPshot | rs677221 |
| SNPdbe | rs677221 |
| MSV3d | rs677221 |
| GWAS Ctlg | rs677221 |
| GMAF | 0.4518 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18708184] Neuregulin 3 genetic variations and susceptibility to schizophrenia in a Chinese population.
[PMID 19118813
] Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.
