rs17511627
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs17511627(A;C) |
Make rs17511627(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 26150190 |
Gene | RNF6 |
is a | snp |
is | mentioned by |
dbSNP | rs17511627 |
dbSNP (classic) | rs17511627 |
ClinGen | rs17511627 |
ebi | rs17511627 |
HLI | rs17511627 |
Exac | rs17511627 |
Gnomad | rs17511627 |
Varsome | rs17511627 |
LitVar | rs17511627 |
Map | rs17511627 |
PheGenI | rs17511627 |
Biobank | rs17511627 |
1000 genomes | rs17511627 |
hgdp | rs17511627 |
ensembl | rs17511627 |
geneview | rs17511627 |
scholar | rs17511627 |
rs17511627 | |
pharmgkb | rs17511627 |
gwascentral | rs17511627 |
openSNP | rs17511627 |
23andMe | rs17511627 |
SNPshot | rs17511627 |
SNPdbe | rs17511627 |
MSV3d | rs17511627 |
GWAS Ctlg | rs17511627 |
GMAF | 0.1837 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22159054] |
Trait | |
Title | A comprehensive genetic association study of Alzheimer disease in African Americans. |
Risk Allele | C |
P-val | 0.000005 |
Odds Ratio | 1.7500 None |