rs267015
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs267015(C;C) |
Make rs267015(C;T) |
Make rs267015(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 155476610 |
is a | snp |
is | mentioned by |
dbSNP | rs267015 |
dbSNP (classic) | rs267015 |
ClinGen | rs267015 |
ebi | rs267015 |
HLI | rs267015 |
Exac | rs267015 |
Gnomad | rs267015 |
Varsome | rs267015 |
LitVar | rs267015 |
Map | rs267015 |
PheGenI | rs267015 |
Biobank | rs267015 |
1000 genomes | rs267015 |
hgdp | rs267015 |
ensembl | rs267015 |
geneview | rs267015 |
scholar | rs267015 |
rs267015 | |
pharmgkb | rs267015 |
gwascentral | rs267015 |
openSNP | rs267015 |
23andMe | rs267015 |
SNPshot | rs267015 |
SNPdbe | rs267015 |
MSV3d | rs267015 |
GWAS Ctlg | rs267015 |
GMAF | 0.1474 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19319892] A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.