rs10035961
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10035961(A;A) |
Make rs10035961(A;C) |
Make rs10035961(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 157603387 |
is a | snp |
is | mentioned by |
dbSNP | rs10035961 |
dbSNP (classic) | rs10035961 |
ClinGen | rs10035961 |
ebi | rs10035961 |
HLI | rs10035961 |
Exac | rs10035961 |
Gnomad | rs10035961 |
Varsome | rs10035961 |
LitVar | rs10035961 |
Map | rs10035961 |
PheGenI | rs10035961 |
Biobank | rs10035961 |
1000 genomes | rs10035961 |
hgdp | rs10035961 |
ensembl | rs10035961 |
geneview | rs10035961 |
scholar | rs10035961 |
rs10035961 | |
pharmgkb | rs10035961 |
gwascentral | rs10035961 |
openSNP | rs10035961 |
23andMe | rs10035961 |
SNPshot | rs10035961 |
SNPdbe | rs10035961 |
MSV3d | rs10035961 |
GWAS Ctlg | rs10035961 |
GMAF | 0.3563 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19319892] A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.