rs6125962
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6125962(C;C) |
Make rs6125962(C;T) |
Make rs6125962(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 37712660 |
Gene | CTNNBL1 |
is a | snp |
is | mentioned by |
dbSNP | rs6125962 |
dbSNP (classic) | rs6125962 |
ClinGen | rs6125962 |
ebi | rs6125962 |
HLI | rs6125962 |
Exac | rs6125962 |
Gnomad | rs6125962 |
Varsome | rs6125962 |
LitVar | rs6125962 |
Map | rs6125962 |
PheGenI | rs6125962 |
Biobank | rs6125962 |
1000 genomes | rs6125962 |
hgdp | rs6125962 |
ensembl | rs6125962 |
geneview | rs6125962 |
scholar | rs6125962 |
rs6125962 | |
pharmgkb | rs6125962 |
gwascentral | rs6125962 |
openSNP | rs6125962 |
23andMe | rs6125962 |
SNPshot | rs6125962 |
SNPdbe | rs6125962 |
MSV3d | rs6125962 |
GWAS Ctlg | rs6125962 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27103528] Association of genetic risk factors with cognitive decline: the PATH through life project.