rs3212172
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3212172(A;A) |
Make rs3212172(A;G) |
Make rs3212172(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 20 |
Position | 44399750 |
Gene | HNF4A |
is a | snp |
is | mentioned by |
dbSNP | rs3212172 |
dbSNP (classic) | rs3212172 |
ClinGen | rs3212172 |
ebi | rs3212172 |
HLI | rs3212172 |
Exac | rs3212172 |
Gnomad | rs3212172 |
Varsome | rs3212172 |
LitVar | rs3212172 |
Map | rs3212172 |
PheGenI | rs3212172 |
Biobank | rs3212172 |
1000 genomes | rs3212172 |
hgdp | rs3212172 |
ensembl | rs3212172 |
geneview | rs3212172 |
scholar | rs3212172 |
rs3212172 | |
pharmgkb | rs3212172 |
gwascentral | rs3212172 |
openSNP | rs3212172 |
23andMe | rs3212172 |
SNPshot | rs3212172 |
SNPdbe | rs3212172 |
MSV3d | rs3212172 |
GWAS Ctlg | rs3212172 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25671620] Hepatocyte Nuclear Factor 4 Alpha Polymorphisms and the Metabolic Syndrome in French-Canadian Youth