rs9943849
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9943849(C;C) |
Make rs9943849(C;T) |
Make rs9943849(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 68976976 |
is a | snp |
is | mentioned by |
dbSNP | rs9943849 |
dbSNP (classic) | rs9943849 |
ClinGen | rs9943849 |
ebi | rs9943849 |
HLI | rs9943849 |
Exac | rs9943849 |
Gnomad | rs9943849 |
Varsome | rs9943849 |
LitVar | rs9943849 |
Map | rs9943849 |
PheGenI | rs9943849 |
Biobank | rs9943849 |
1000 genomes | rs9943849 |
hgdp | rs9943849 |
ensembl | rs9943849 |
geneview | rs9943849 |
scholar | rs9943849 |
rs9943849 | |
pharmgkb | rs9943849 |
gwascentral | rs9943849 |
openSNP | rs9943849 |
23andMe | rs9943849 |
SNPshot | rs9943849 |
SNPdbe | rs9943849 |
MSV3d | rs9943849 |
GWAS Ctlg | rs9943849 |
GMAF | 0.2406 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20673876] Genome-Wide Association-, Replication-, and Neuroimaging Study Implicates HOMER1 in the Etiology of Major Depression