rs716595
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs716595(A;A) |
Make rs716595(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 110246728 |
Gene | MXI1 |
is a | snp |
is | mentioned by |
dbSNP | rs716595 |
dbSNP (classic) | rs716595 |
ClinGen | rs716595 |
ebi | rs716595 |
HLI | rs716595 |
Exac | rs716595 |
Gnomad | rs716595 |
Varsome | rs716595 |
LitVar | rs716595 |
Map | rs716595 |
PheGenI | rs716595 |
Biobank | rs716595 |
1000 genomes | rs716595 |
hgdp | rs716595 |
ensembl | rs716595 |
geneview | rs716595 |
scholar | rs716595 |
rs716595 | |
pharmgkb | rs716595 |
gwascentral | rs716595 |
openSNP | rs716595 |
23andMe | rs716595 |
SNPshot | rs716595 |
SNPdbe | rs716595 |
MSV3d | rs716595 |
GWAS Ctlg | rs716595 |
GMAF | 0.1483 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19010793] |
Trait | Normalized brain volume |
Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | NR NR |