rs6750634
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6750634(A;A) |
Make rs6750634(A;G) |
Make rs6750634(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 50533365 |
Gene | NRXN1 |
is a | snp |
is | mentioned by |
dbSNP | rs6750634 |
dbSNP (classic) | rs6750634 |
ClinGen | rs6750634 |
ebi | rs6750634 |
HLI | rs6750634 |
Exac | rs6750634 |
Gnomad | rs6750634 |
Varsome | rs6750634 |
LitVar | rs6750634 |
Map | rs6750634 |
PheGenI | rs6750634 |
Biobank | rs6750634 |
1000 genomes | rs6750634 |
hgdp | rs6750634 |
ensembl | rs6750634 |
geneview | rs6750634 |
scholar | rs6750634 |
rs6750634 | |
pharmgkb | rs6750634 |
gwascentral | rs6750634 |
openSNP | rs6750634 |
23andMe | rs6750634 |
SNPshot | rs6750634 |
SNPdbe | rs6750634 |
MSV3d | rs6750634 |
GWAS Ctlg | rs6750634 |
GMAF | 0.3815 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23319000] |
Trait | Metabolite levels (HVA/MHPG ratio) |
Title | Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. |
Risk Allele | A |
P-val | 4E-6 |
Odds Ratio | .29 unit decrease |