rs1558477
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1558477(C;C) |
Make rs1558477(C;T) |
Make rs1558477(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 31115733 |
is a | snp |
is | mentioned by |
dbSNP | rs1558477 |
dbSNP (classic) | rs1558477 |
ClinGen | rs1558477 |
ebi | rs1558477 |
HLI | rs1558477 |
Exac | rs1558477 |
Gnomad | rs1558477 |
Varsome | rs1558477 |
LitVar | rs1558477 |
Map | rs1558477 |
PheGenI | rs1558477 |
Biobank | rs1558477 |
1000 genomes | rs1558477 |
hgdp | rs1558477 |
ensembl | rs1558477 |
geneview | rs1558477 |
scholar | rs1558477 |
rs1558477 | |
pharmgkb | rs1558477 |
gwascentral | rs1558477 |
openSNP | rs1558477 |
23andMe | rs1558477 |
SNPshot | rs1558477 |
SNPdbe | rs1558477 |
MSV3d | rs1558477 |
GWAS Ctlg | rs1558477 |
GMAF | 0.3545 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21621269] |
Trait | |
Title | Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. |
Risk Allele | |
P-val | 3E-7 |
Odds Ratio | None None |
[PMID 19065144] Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo.