rs11466314
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs11466314(A;A) |
Make rs11466314(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 41354331 |
Gene | B9D2, TGFB1 |
is a | snp |
is | mentioned by |
dbSNP | rs11466314 |
dbSNP (classic) | rs11466314 |
ClinGen | rs11466314 |
ebi | rs11466314 |
HLI | rs11466314 |
Exac | rs11466314 |
Gnomad | rs11466314 |
Varsome | rs11466314 |
LitVar | rs11466314 |
Map | rs11466314 |
PheGenI | rs11466314 |
Biobank | rs11466314 |
1000 genomes | rs11466314 |
hgdp | rs11466314 |
ensembl | rs11466314 |
geneview | rs11466314 |
scholar | rs11466314 |
rs11466314 | |
pharmgkb | rs11466314 |
gwascentral | rs11466314 |
openSNP | rs11466314 |
23andMe | rs11466314 |
SNPshot | rs11466314 |
SNPdbe | rs11466314 |
MSV3d | rs11466314 |
GWAS Ctlg | rs11466314 |
GMAF | 0.003214 |
Max Magnitude | 0 |
[PMID 18366677] Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission.