rs4810424
Orientation | plus |
Stabilized | plus |
Make rs4810424(C;C) |
Make rs4810424(C;G) |
Make rs4810424(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 44346383 |
Gene | R3HDML |
is a | snp |
is | mentioned by |
dbSNP | rs4810424 |
dbSNP (classic) | rs4810424 |
ClinGen | rs4810424 |
ebi | rs4810424 |
HLI | rs4810424 |
Exac | rs4810424 |
Gnomad | rs4810424 |
Varsome | rs4810424 |
LitVar | rs4810424 |
Map | rs4810424 |
PheGenI | rs4810424 |
Biobank | rs4810424 |
1000 genomes | rs4810424 |
hgdp | rs4810424 |
ensembl | rs4810424 |
geneview | rs4810424 |
scholar | rs4810424 |
rs4810424 | |
pharmgkb | rs4810424 |
gwascentral | rs4810424 |
openSNP | rs4810424 |
23andMe | rs4810424 |
SNPshot | rs4810424 |
SNPdbe | rs4810424 |
MSV3d | rs4810424 |
GWAS Ctlg | rs4810424 |
GMAF | 0.2466 |
Max Magnitude | 0 |
[PMID 19748811] Influence of hepatocyte nuclear factor 4alpha (HNF4alpha) gene variants on the risk of type 2 diabetes: A meta-analysis in 49,577 individuals
[PMID 21633728] Hepatocyte nuclear factor 4 alpha P2 promoter variants associate with insulin resistance
[PMID 21983932] Association of Hepatocyte Nuclear Factor 4 Alpha Polymorphisms with Type 2 Diabetes With or Without Metabolic Syndrome in Malaysia[PMID 15504983] Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population.
[PMID 16186411] Variants in hepatocyte nuclear factor 4alpha are modestly associated with type 2 diabetes in Pima Indians.
[PMID 16523192] Polymorphisms in the gene encoding hepatocyte nuclear factor-4alpha and susceptibility to type 2 diabetes in a Polish population.
[PMID 16838170] Single nucleotide polymorphisms of the HNF4alpha gene are associated with the conversion to type 2 diabetes mellitus: the STOP-NIDDM trial.
[PMID 17894829] Gene-gene interactions between HNF4A and KCNJ11 in predicting Type 2 diabetes in women.
[PMID 18332101] Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes.
[PMID 18654799] Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.
[PMID 18728231] Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies.