rs3850333
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3850333(C;C) |
Make rs3850333(C;T) |
Make rs3850333(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 50775791 |
Gene | NRXN1 |
is a | snp |
is | mentioned by |
dbSNP | rs3850333 |
dbSNP (classic) | rs3850333 |
ClinGen | rs3850333 |
ebi | rs3850333 |
HLI | rs3850333 |
Exac | rs3850333 |
Gnomad | rs3850333 |
Varsome | rs3850333 |
LitVar | rs3850333 |
Map | rs3850333 |
PheGenI | rs3850333 |
Biobank | rs3850333 |
1000 genomes | rs3850333 |
hgdp | rs3850333 |
ensembl | rs3850333 |
geneview | rs3850333 |
scholar | rs3850333 |
rs3850333 | |
pharmgkb | rs3850333 |
gwascentral | rs3850333 |
openSNP | rs3850333 |
23andMe | rs3850333 |
SNPshot | rs3850333 |
SNPdbe | rs3850333 |
MSV3d | rs3850333 |
GWAS Ctlg | rs3850333 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25124521] Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain