rs17178006
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs17178006(G;G) |
Make rs17178006(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 65324519 |
Gene | MSRB3 |
is a | snp |
is | mentioned by |
dbSNP | rs17178006 |
dbSNP (classic) | rs17178006 |
ClinGen | rs17178006 |
ebi | rs17178006 |
HLI | rs17178006 |
Exac | rs17178006 |
Gnomad | rs17178006 |
Varsome | rs17178006 |
LitVar | rs17178006 |
Map | rs17178006 |
PheGenI | rs17178006 |
Biobank | rs17178006 |
1000 genomes | rs17178006 |
hgdp | rs17178006 |
ensembl | rs17178006 |
geneview | rs17178006 |
scholar | rs17178006 |
rs17178006 | |
pharmgkb | rs17178006 |
gwascentral | rs17178006 |
openSNP | rs17178006 |
23andMe | rs17178006 |
SNPshot | rs17178006 |
SNPdbe | rs17178006 |
MSV3d | rs17178006 |
GWAS Ctlg | rs17178006 |
GMAF | 0.03903 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 22504421] Common variants at 12q14 and 12q24 are associated with hippocampal volume