rs3824886
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs3824886(G;T) |
Make rs3824886(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 20383067 |
Gene | HTATIP2 |
is a | snp |
is | mentioned by |
dbSNP | rs3824886 |
dbSNP (classic) | rs3824886 |
ClinGen | rs3824886 |
ebi | rs3824886 |
HLI | rs3824886 |
Exac | rs3824886 |
Gnomad | rs3824886 |
Varsome | rs3824886 |
LitVar | rs3824886 |
Map | rs3824886 |
PheGenI | rs3824886 |
Biobank | rs3824886 |
1000 genomes | rs3824886 |
hgdp | rs3824886 |
ensembl | rs3824886 |
geneview | rs3824886 |
scholar | rs3824886 |
rs3824886 | |
pharmgkb | rs3824886 |
gwascentral | rs3824886 |
openSNP | rs3824886 |
23andMe | rs3824886 |
SNPshot | rs3824886 |
SNPdbe | rs3824886 |
MSV3d | rs3824886 |
GWAS Ctlg | rs3824886 |
GMAF | 0.2888 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 16251468] Survey of allelic expression using EST mining.