rs12474969
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12474969(A;A) |
Make rs12474969(A;G) |
Make rs12474969(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 9556938 |
Gene | ADAM17 |
is a | snp |
is | mentioned by |
dbSNP | rs12474969 |
dbSNP (classic) | rs12474969 |
ClinGen | rs12474969 |
ebi | rs12474969 |
HLI | rs12474969 |
Exac | rs12474969 |
Gnomad | rs12474969 |
Varsome | rs12474969 |
LitVar | rs12474969 |
Map | rs12474969 |
PheGenI | rs12474969 |
Biobank | rs12474969 |
1000 genomes | rs12474969 |
hgdp | rs12474969 |
ensembl | rs12474969 |
geneview | rs12474969 |
scholar | rs12474969 |
rs12474969 | |
pharmgkb | rs12474969 |
gwascentral | rs12474969 |
openSNP | rs12474969 |
23andMe | rs12474969 |
SNPshot | rs12474969 |
SNPdbe | rs12474969 |
MSV3d | rs12474969 |
GWAS Ctlg | rs12474969 |
GMAF | 0.1566 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20627730] The relationship between ADAM17 promoter polymorphisms and sporadic Alzheimer's disease in a Northern Chinese Han population