rs11808092
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs11808092(A;A) |
Make rs11808092(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 92607671 |
Gene | EVI5 |
is a | snp |
is | mentioned by |
dbSNP | rs11808092 |
dbSNP (classic) | rs11808092 |
ClinGen | rs11808092 |
ebi | rs11808092 |
HLI | rs11808092 |
Exac | rs11808092 |
Gnomad | rs11808092 |
Varsome | rs11808092 |
LitVar | rs11808092 |
Map | rs11808092 |
PheGenI | rs11808092 |
Biobank | rs11808092 |
1000 genomes | rs11808092 |
hgdp | rs11808092 |
ensembl | rs11808092 |
geneview | rs11808092 |
scholar | rs11808092 |
rs11808092 | |
pharmgkb | rs11808092 |
gwascentral | rs11808092 |
openSNP | rs11808092 |
23andMe | rs11808092 |
SNPshot | rs11808092 |
SNPdbe | rs11808092 |
MSV3d | rs11808092 |
GWAS Ctlg | rs11808092 |
GMAF | 0.1478 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 20087403] Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
ClinVar | |
---|---|
Risk | rs11808092(A;A) |
Alt | rs11808092(A;A) |
Reference | Rs11808092(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | EVI5 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.93073228C>A |
CLNSRC | |
CLNACC | RCV000455680.1, |