rs2196447
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2196447(A;A) |
Make rs2196447(A;G) |
Make rs2196447(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 79484145 |
Gene | NRXN3 |
is a | snp |
is | mentioned by |
dbSNP | rs2196447 |
dbSNP (classic) | rs2196447 |
ClinGen | rs2196447 |
ebi | rs2196447 |
HLI | rs2196447 |
Exac | rs2196447 |
Gnomad | rs2196447 |
Varsome | rs2196447 |
LitVar | rs2196447 |
Map | rs2196447 |
PheGenI | rs2196447 |
Biobank | rs2196447 |
1000 genomes | rs2196447 |
hgdp | rs2196447 |
ensembl | rs2196447 |
geneview | rs2196447 |
scholar | rs2196447 |
rs2196447 | |
pharmgkb | rs2196447 |
gwascentral | rs2196447 |
openSNP | rs2196447 |
23andMe | rs2196447 |
SNPshot | rs2196447 |
SNPdbe | rs2196447 |
MSV3d | rs2196447 |
GWAS Ctlg | rs2196447 |
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