rs9574199
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs9574199(A;A) |
Make rs9574199(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 78234779 |
Gene | RNF219-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs9574199 |
dbSNP (classic) | rs9574199 |
ClinGen | rs9574199 |
ebi | rs9574199 |
HLI | rs9574199 |
Exac | rs9574199 |
Gnomad | rs9574199 |
Varsome | rs9574199 |
LitVar | rs9574199 |
Map | rs9574199 |
PheGenI | rs9574199 |
Biobank | rs9574199 |
1000 genomes | rs9574199 |
hgdp | rs9574199 |
ensembl | rs9574199 |
geneview | rs9574199 |
scholar | rs9574199 |
rs9574199 | |
pharmgkb | rs9574199 |
gwascentral | rs9574199 |
openSNP | rs9574199 |
23andMe | rs9574199 |
SNPshot | rs9574199 |
SNPdbe | rs9574199 |
MSV3d | rs9574199 |
GWAS Ctlg | rs9574199 |
GMAF | 0.4848 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21116278] |
Trait | |
Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | 0.0041 [NR] unit increase (interaction) |