rs3741208
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3741208(C;C) |
Make rs3741208(C;T) |
Make rs3741208(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2148544 |
Gene | IGF2, IGF2-AS, INS-IGF2 |
is a | snp |
is | mentioned by |
dbSNP | rs3741208 |
dbSNP (classic) | rs3741208 |
ClinGen | rs3741208 |
ebi | rs3741208 |
HLI | rs3741208 |
Exac | rs3741208 |
Gnomad | rs3741208 |
Varsome | rs3741208 |
LitVar | rs3741208 |
Map | rs3741208 |
PheGenI | rs3741208 |
Biobank | rs3741208 |
1000 genomes | rs3741208 |
hgdp | rs3741208 |
ensembl | rs3741208 |
geneview | rs3741208 |
scholar | rs3741208 |
rs3741208 | |
pharmgkb | rs3741208 |
gwascentral | rs3741208 |
openSNP | rs3741208 |
23andMe | rs3741208 |
SNPshot | rs3741208 |
SNPdbe | rs3741208 |
MSV3d | rs3741208 |
GWAS Ctlg | rs3741208 |
GMAF | 0.3421 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 17554260] associated with type-1 diabetes
[PMID 17980034] Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'.
[PMID 19639606] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 19956101] Overview of the Rapid Response data.
[PMID 19956106] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.
[PMID 20403199] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.