rs7116190
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7116190(A;A) |
Make rs7116190(A;G) |
Make rs7116190(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 11 |
Position | 60197519 |
is a | snp |
is | mentioned by |
dbSNP | rs7116190 |
dbSNP (classic) | rs7116190 |
ClinGen | rs7116190 |
ebi | rs7116190 |
HLI | rs7116190 |
Exac | rs7116190 |
Gnomad | rs7116190 |
Varsome | rs7116190 |
LitVar | rs7116190 |
Map | rs7116190 |
PheGenI | rs7116190 |
Biobank | rs7116190 |
1000 genomes | rs7116190 |
hgdp | rs7116190 |
ensembl | rs7116190 |
geneview | rs7116190 |
scholar | rs7116190 |
rs7116190 | |
pharmgkb | rs7116190 |
gwascentral | rs7116190 |
openSNP | rs7116190 |
23andMe | rs7116190 |
SNPshot | rs7116190 |
SNPdbe | rs7116190 |
MSV3d | rs7116190 |
GWAS Ctlg | rs7116190 |
Max Magnitude | 0 |
[PMID 28323831] Alzheimer's disease polygenic hazard score