rs7849530
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7849530(A;A) |
Make rs7849530(A;G) |
Make rs7849530(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 92165453 |
is a | snp |
is | mentioned by |
dbSNP | rs7849530 |
dbSNP (classic) | rs7849530 |
ClinGen | rs7849530 |
ebi | rs7849530 |
HLI | rs7849530 |
Exac | rs7849530 |
Gnomad | rs7849530 |
Varsome | rs7849530 |
LitVar | rs7849530 |
Map | rs7849530 |
PheGenI | rs7849530 |
Biobank | rs7849530 |
1000 genomes | rs7849530 |
hgdp | rs7849530 |
ensembl | rs7849530 |
geneview | rs7849530 |
scholar | rs7849530 |
rs7849530 | |
pharmgkb | rs7849530 |
gwascentral | rs7849530 |
openSNP | rs7849530 |
23andMe | rs7849530 |
SNPshot | rs7849530 |
SNPdbe | rs7849530 |
MSV3d | rs7849530 |
GWAS Ctlg | rs7849530 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25140149] Genetic variation modifies risk for neurodegeneration based on biomarker status