rs10497511
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs10497511(C;C) |
Make rs10497511(C;T) |
Make rs10497511(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 177254568 |
Gene | NFE2L2 |
is a | snp |
is | mentioned by |
dbSNP | rs10497511 |
dbSNP (classic) | rs10497511 |
ClinGen | rs10497511 |
ebi | rs10497511 |
HLI | rs10497511 |
Exac | rs10497511 |
Gnomad | rs10497511 |
Varsome | rs10497511 |
LitVar | rs10497511 |
Map | rs10497511 |
PheGenI | rs10497511 |
Biobank | rs10497511 |
1000 genomes | rs10497511 |
hgdp | rs10497511 |
ensembl | rs10497511 |
geneview | rs10497511 |
scholar | rs10497511 |
rs10497511 | |
pharmgkb | rs10497511 |
gwascentral | rs10497511 |
openSNP | rs10497511 |
23andMe | rs10497511 |
SNPshot | rs10497511 |
SNPdbe | rs10497511 |
MSV3d | rs10497511 |
GWAS Ctlg | rs10497511 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27374075] Genetic variants of nuclear factor erythroid-derived 2-like 2 associated with the complications in Han descents with type 2 diabetes mellitus of Northeast China.