rs10103191
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10103191(A;A) |
Make rs10103191(A;G) |
Make rs10103191(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 91890204 |
is a | snp |
is | mentioned by |
dbSNP | rs10103191 |
dbSNP (classic) | rs10103191 |
ClinGen | rs10103191 |
ebi | rs10103191 |
HLI | rs10103191 |
Exac | rs10103191 |
Gnomad | rs10103191 |
Varsome | rs10103191 |
LitVar | rs10103191 |
Map | rs10103191 |
PheGenI | rs10103191 |
Biobank | rs10103191 |
1000 genomes | rs10103191 |
hgdp | rs10103191 |
ensembl | rs10103191 |
geneview | rs10103191 |
scholar | rs10103191 |
rs10103191 | |
pharmgkb | rs10103191 |
gwascentral | rs10103191 |
openSNP | rs10103191 |
23andMe | rs10103191 |
SNPshot | rs10103191 |
SNPdbe | rs10103191 |
MSV3d | rs10103191 |
GWAS Ctlg | rs10103191 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29225345] Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.