rs749005
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs749005(A;A) |
Make rs749005(A;C) |
Make rs749005(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 6283433 |
Gene | F13A1 |
is a | snp |
is | mentioned by |
dbSNP | rs749005 |
dbSNP (classic) | rs749005 |
ClinGen | rs749005 |
ebi | rs749005 |
HLI | rs749005 |
Exac | rs749005 |
Gnomad | rs749005 |
Varsome | rs749005 |
LitVar | rs749005 |
Map | rs749005 |
PheGenI | rs749005 |
Biobank | rs749005 |
1000 genomes | rs749005 |
hgdp | rs749005 |
ensembl | rs749005 |
geneview | rs749005 |
scholar | rs749005 |
rs749005 | |
pharmgkb | rs749005 |
gwascentral | rs749005 |
openSNP | rs749005 |
23andMe | rs749005 |
SNPshot | rs749005 |
SNPdbe | rs749005 |
MSV3d | rs749005 |
GWAS Ctlg | rs749005 |
GMAF | 0.1373 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21116278] |
Trait | |
Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
Risk Allele | |
P-val | 3E-7 |
Odds Ratio | 0.0002 [NR] unit decrease (main effect) |