rs2607474
From SNPedia
Merged into | rs1838720 |
Orientation | minus |
Stabilized | minus |
Make rs2607474(A;A) |
Make rs2607474(A;G) |
Make rs2607474(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 59303563 |
Gene | PDE4D |
is a | snp |
is | mentioned by |
dbSNP | rs2607474 |
dbSNP (classic) | rs2607474 |
ClinGen | rs2607474 |
ebi | rs2607474 |
HLI | rs2607474 |
Exac | rs2607474 |
Gnomad | rs2607474 |
Varsome | rs2607474 |
LitVar | rs2607474 |
Map | rs2607474 |
PheGenI | rs2607474 |
Biobank | rs2607474 |
1000 genomes | rs2607474 |
hgdp | rs2607474 |
ensembl | rs2607474 |
geneview | rs2607474 |
scholar | rs2607474 |
rs2607474 | |
pharmgkb | rs2607474 |
gwascentral | rs2607474 |
openSNP | rs2607474 |
23andMe | rs2607474 |
SNPshot | rs2607474 |
SNPdbe | rs2607474 |
MSV3d | rs2607474 |
GWAS Ctlg | rs2607474 |
Status | Merged into rs1838720 |
Max Magnitude | 0 |
[PMID 22720301] Effects of -1018G>A polymorphism of HRH2 (rs2607474) on the severity of gastric mucosal atrophy
[PMID 23280118] Influence of HRH2 promoter polymorphism on aberrant DNA methylation of DAPK and CDH1 in the gastric epithelium