rs945270
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs945270(C;C) |
Make rs945270(C;G) |
Make rs945270(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 14 |
Position | 55733755 |
Gene | KTN1 |
is a | snp |
is | mentioned by |
dbSNP | rs945270 |
dbSNP (classic) | rs945270 |
ClinGen | rs945270 |
ebi | rs945270 |
HLI | rs945270 |
Exac | rs945270 |
Gnomad | rs945270 |
Varsome | rs945270 |
LitVar | rs945270 |
Map | rs945270 |
PheGenI | rs945270 |
Biobank | rs945270 |
1000 genomes | rs945270 |
hgdp | rs945270 |
ensembl | rs945270 |
geneview | rs945270 |
scholar | rs945270 |
rs945270 | |
pharmgkb | rs945270 |
gwascentral | rs945270 |
openSNP | rs945270 |
23andMe | rs945270 |
SNPshot | rs945270 |
SNPdbe | rs945270 |
MSV3d | rs945270 |
GWAS Ctlg | rs945270 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 25607358] Common genetic variants influence human subcortical brain structures.