rs3811463
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3811463(A;A) |
Make rs3811463(A;G) |
Make rs3811463(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 26427451 |
Gene | LIN28A |
is a | snp |
is | mentioned by |
dbSNP | rs3811463 |
dbSNP (classic) | rs3811463 |
ClinGen | rs3811463 |
ebi | rs3811463 |
HLI | rs3811463 |
Exac | rs3811463 |
Gnomad | rs3811463 |
Varsome | rs3811463 |
LitVar | rs3811463 |
Map | rs3811463 |
PheGenI | rs3811463 |
Biobank | rs3811463 |
1000 genomes | rs3811463 |
hgdp | rs3811463 |
ensembl | rs3811463 |
geneview | rs3811463 |
scholar | rs3811463 |
rs3811463 | |
pharmgkb | rs3811463 |
gwascentral | rs3811463 |
openSNP | rs3811463 |
23andMe | rs3811463 |
SNPshot | rs3811463 |
SNPdbe | rs3811463 |
MSV3d | rs3811463 |
GWAS Ctlg | rs3811463 |
GMAF | 0.3577 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23660113] The polymorphism in the let-7 targeted region of the Lin28 gene is associated with increased risk of type 2 diabetes mellitus
[PMID 29201231] Genetic variation of rs3811463 is associated with gestational diabetes mellitus susceptibility.