rs17006206
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs17006206(A;G) |
Make rs17006206(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 27684606 |
Gene | SLC4A1AP |
is a | snp |
is | mentioned by |
dbSNP | rs17006206 |
dbSNP (classic) | rs17006206 |
ClinGen | rs17006206 |
ebi | rs17006206 |
HLI | rs17006206 |
Exac | rs17006206 |
Gnomad | rs17006206 |
Varsome | rs17006206 |
LitVar | rs17006206 |
Map | rs17006206 |
PheGenI | rs17006206 |
Biobank | rs17006206 |
1000 genomes | rs17006206 |
hgdp | rs17006206 |
ensembl | rs17006206 |
geneview | rs17006206 |
scholar | rs17006206 |
rs17006206 | |
pharmgkb | rs17006206 |
gwascentral | rs17006206 |
openSNP | rs17006206 |
23andMe | rs17006206 |
SNPshot | rs17006206 |
SNPdbe | rs17006206 |
MSV3d | rs17006206 |
GWAS Ctlg | rs17006206 |
GMAF | 0.0202 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22159054] |
Trait | |
Title | A comprehensive genetic association study of Alzheimer disease in African Americans. |
Risk Allele | G |
P-val | 0.000002 |
Odds Ratio | 2.0500 None |