rs10790256
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10790256(C;C) |
Make rs10790256(C;T) |
Make rs10790256(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 118663373 |
Gene | TREH |
is a | snp |
is | mentioned by |
dbSNP | rs10790256 |
dbSNP (classic) | rs10790256 |
ClinGen | rs10790256 |
ebi | rs10790256 |
HLI | rs10790256 |
Exac | rs10790256 |
Gnomad | rs10790256 |
Varsome | rs10790256 |
LitVar | rs10790256 |
Map | rs10790256 |
PheGenI | rs10790256 |
Biobank | rs10790256 |
1000 genomes | rs10790256 |
hgdp | rs10790256 |
ensembl | rs10790256 |
geneview | rs10790256 |
scholar | rs10790256 |
rs10790256 | |
pharmgkb | rs10790256 |
gwascentral | rs10790256 |
openSNP | rs10790256 |
23andMe | rs10790256 |
SNPshot | rs10790256 |
SNPdbe | rs10790256 |
MSV3d | rs10790256 |
GWAS Ctlg | rs10790256 |
GMAF | 0.1736 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23468175] Identification of genetic variation that determines human trehalase activity and its association with type 2 diabetes