rs1927457
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1927457(C;C) |
Make rs1927457(C;T) |
Make rs1927457(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 29719734 |
Gene | SVIL |
is a | snp |
is | mentioned by |
dbSNP | rs1927457 |
dbSNP (classic) | rs1927457 |
ClinGen | rs1927457 |
ebi | rs1927457 |
HLI | rs1927457 |
Exac | rs1927457 |
Gnomad | rs1927457 |
Varsome | rs1927457 |
LitVar | rs1927457 |
Map | rs1927457 |
PheGenI | rs1927457 |
Biobank | rs1927457 |
1000 genomes | rs1927457 |
hgdp | rs1927457 |
ensembl | rs1927457 |
geneview | rs1927457 |
scholar | rs1927457 |
rs1927457 | |
pharmgkb | rs1927457 |
gwascentral | rs1927457 |
openSNP | rs1927457 |
23andMe | rs1927457 |
SNPshot | rs1927457 |
SNPdbe | rs1927457 |
MSV3d | rs1927457 |
GWAS Ctlg | rs1927457 |
GMAF | 0.3852 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 |