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