rs3754860
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3754860(C;C) |
Make rs3754860(C;T) |
Make rs3754860(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 25170385 |
Gene | POMC |
is a | snp |
is | mentioned by |
dbSNP | rs3754860 |
dbSNP (classic) | rs3754860 |
ClinGen | rs3754860 |
ebi | rs3754860 |
HLI | rs3754860 |
Exac | rs3754860 |
Gnomad | rs3754860 |
Varsome | rs3754860 |
LitVar | rs3754860 |
Map | rs3754860 |
PheGenI | rs3754860 |
Biobank | rs3754860 |
1000 genomes | rs3754860 |
hgdp | rs3754860 |
ensembl | rs3754860 |
geneview | rs3754860 |
scholar | rs3754860 |
rs3754860 | |
pharmgkb | rs3754860 |
gwascentral | rs3754860 |
openSNP | rs3754860 |
23andMe | rs3754860 |
SNPshot | rs3754860 |
SNPdbe | rs3754860 |
MSV3d | rs3754860 |
GWAS Ctlg | rs3754860 |
GMAF | 0.219 |
Max Magnitude | 0 |
[PMID 21723177] Association analysis of proopiomelanocortin (POMC) haplotypes in type 1 diabetes in a UK population [PMID 19337797] Association between variants in the genes for leptin, leptin receptor, and proopiomelanocortin with chronic heart failure in the Czech population.