rs116348108
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common genotype |
Make rs116348108(A;G) |
Make rs116348108(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 119099432 |
Gene | DMXL1 |
is a | snp |
is | mentioned by |
dbSNP | rs116348108 |
dbSNP (classic) | rs116348108 |
ClinGen | rs116348108 |
ebi | rs116348108 |
HLI | rs116348108 |
Exac | rs116348108 |
Gnomad | rs116348108 |
Varsome | rs116348108 |
LitVar | rs116348108 |
Map | rs116348108 |
PheGenI | rs116348108 |
Biobank | rs116348108 |
1000 genomes | rs116348108 |
hgdp | rs116348108 |
ensembl | rs116348108 |
geneview | rs116348108 |
scholar | rs116348108 |
rs116348108 | |
pharmgkb | rs116348108 |
gwascentral | rs116348108 |
openSNP | rs116348108 |
23andMe | rs116348108 |
SNPshot | rs116348108 |
SNPdbe | rs116348108 |
MSV3d | rs116348108 |
GWAS Ctlg | rs116348108 |
GMAF | 0.01286 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23535033] |
Trait | Alzheimer's disease (cognitive decline) |
Title | Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. |
Risk Allele | |
P-val | 9E-7 |
Odds Ratio | .28 unit decrease |