rs10276619
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10276619(A;A) |
Make rs10276619(A;G) |
Make rs10276619(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 50273756 |
is a | snp |
is | mentioned by |
dbSNP | rs10276619 |
dbSNP (classic) | rs10276619 |
ClinGen | rs10276619 |
ebi | rs10276619 |
HLI | rs10276619 |
Exac | rs10276619 |
Gnomad | rs10276619 |
Varsome | rs10276619 |
LitVar | rs10276619 |
Map | rs10276619 |
PheGenI | rs10276619 |
Biobank | rs10276619 |
1000 genomes | rs10276619 |
hgdp | rs10276619 |
ensembl | rs10276619 |
geneview | rs10276619 |
scholar | rs10276619 |
rs10276619 | |
pharmgkb | rs10276619 |
gwascentral | rs10276619 |
openSNP | rs10276619 |
23andMe | rs10276619 |
SNPshot | rs10276619 |
SNPdbe | rs10276619 |
MSV3d | rs10276619 |
GWAS Ctlg | rs10276619 |
GMAF | 0.4541 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19668339] |
Trait | Hippocampal atrophy |
Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | NR NR |
GWAS snp | |
---|---|
PMID | [PMID 23273568] |
Trait | Systemic lupus erythematosus |
Title | Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. |
Risk Allele | G |
P-val | 6E-6 |
Odds Ratio | 1.18 |