rs11845632
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11845632(A;A) |
| Make rs11845632(A;G) |
| Make rs11845632(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 79487471 |
| Gene | NRXN3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11845632 |
| dbSNP (classic) | rs11845632 |
| ClinGen | rs11845632 |
| ebi | rs11845632 |
| HLI | rs11845632 |
| Exac | rs11845632 |
| Gnomad | rs11845632 |
| Varsome | rs11845632 |
| LitVar | rs11845632 |
| Map | rs11845632 |
| PheGenI | rs11845632 |
| Biobank | rs11845632 |
| 1000 genomes | rs11845632 |
| hgdp | rs11845632 |
| ensembl | rs11845632 |
| geneview | rs11845632 |
| scholar | rs11845632 |
| rs11845632 | |
| pharmgkb | rs11845632 |
| gwascentral | rs11845632 |
| openSNP | rs11845632 |
| 23andMe | rs11845632 |
| SNPshot | rs11845632 |
| SNPdbe | rs11845632 |
| MSV3d | rs11845632 |
| GWAS Ctlg | rs11845632 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24265751
] DNA pooling base genome-wide association study identifies variants at NRXN3 associated with delayed encephalopathy after acute carbon monoxide poisoning
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 14
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
