rs6741949
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6741949(C;C) |
Make rs6741949(C;G) |
Make rs6741949(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 162053713 |
Gene | DPP4 |
is a | snp |
is | mentioned by |
dbSNP | rs6741949 |
dbSNP (classic) | rs6741949 |
ClinGen | rs6741949 |
ebi | rs6741949 |
HLI | rs6741949 |
Exac | rs6741949 |
Gnomad | rs6741949 |
Varsome | rs6741949 |
LitVar | rs6741949 |
Map | rs6741949 |
PheGenI | rs6741949 |
Biobank | rs6741949 |
1000 genomes | rs6741949 |
hgdp | rs6741949 |
ensembl | rs6741949 |
geneview | rs6741949 |
scholar | rs6741949 |
rs6741949 | |
pharmgkb | rs6741949 |
gwascentral | rs6741949 |
openSNP | rs6741949 |
23andMe | rs6741949 |
SNPshot | rs6741949 |
SNPdbe | rs6741949 |
MSV3d | rs6741949 |
GWAS Ctlg | rs6741949 |
GMAF | 0.2622 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22504421] Common variants at 12q14 and 12q24 are associated with hippocampal volume