rs879471
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs879471(C;C) |
Make rs879471(C;T) |
Make rs879471(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 63638589 |
Gene | STMN3 |
is a | snp |
is | mentioned by |
dbSNP | rs879471 |
dbSNP (classic) | rs879471 |
ClinGen | rs879471 |
ebi | rs879471 |
HLI | rs879471 |
Exac | rs879471 |
Gnomad | rs879471 |
Varsome | rs879471 |
LitVar | rs879471 |
Map | rs879471 |
PheGenI | rs879471 |
Biobank | rs879471 |
1000 genomes | rs879471 |
hgdp | rs879471 |
ensembl | rs879471 |
geneview | rs879471 |
scholar | rs879471 |
rs879471 | |
pharmgkb | rs879471 |
gwascentral | rs879471 |
openSNP | rs879471 |
23andMe | rs879471 |
SNPshot | rs879471 |
SNPdbe | rs879471 |
MSV3d | rs879471 |
GWAS Ctlg | rs879471 |
GMAF | 0.3407 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23091480] Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach