rs296766
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(T;T) | 0 | common in clinvar |
Make rs296766(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 49957170 |
Gene | AQP2, LOC101927318 |
is a | snp |
is | mentioned by |
dbSNP | rs296766 |
dbSNP (classic) | rs296766 |
ClinGen | rs296766 |
ebi | rs296766 |
HLI | rs296766 |
Exac | rs296766 |
Gnomad | rs296766 |
Varsome | rs296766 |
LitVar | rs296766 |
Map | rs296766 |
PheGenI | rs296766 |
Biobank | rs296766 |
1000 genomes | rs296766 |
hgdp | rs296766 |
ensembl | rs296766 |
geneview | rs296766 |
scholar | rs296766 |
rs296766 | |
pharmgkb | rs296766 |
gwascentral | rs296766 |
openSNP | rs296766 |
23andMe | rs296766 |
SNPshot | rs296766 |
SNPdbe | rs296766 |
MSV3d | rs296766 |
GWAS Ctlg | rs296766 |
GMAF | 0.1084 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21934636] Genetic predisposition and nongenetic risk factors of thiazolidinedione-related edema in patients with type 2 diabetes
ClinVar | |
---|---|
Risk | Rs296766(C;C) |
Alt | Rs296766(C;C) |
Reference | Rs296766(T;T) |
Significance | Non-pathogenic |
Disease | Nephrogenic diabetes insipidus |
Variation | info |
Gene | AQP2 LOC101927318 |
CLNDBN | Nephrogenic diabetes insipidus |
Reversed | 0 |
HGVS | NC_000012.11:g.50350953T>C |
CLNSRC | |
CLNACC | RCV000386906.1, |