rs4434423
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4434423(A;A) |
Make rs4434423(A;T) |
Make rs4434423(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 40677580 |
is a | snp |
is | mentioned by |
dbSNP | rs4434423 |
dbSNP (classic) | rs4434423 |
ClinGen | rs4434423 |
ebi | rs4434423 |
HLI | rs4434423 |
Exac | rs4434423 |
Gnomad | rs4434423 |
Varsome | rs4434423 |
LitVar | rs4434423 |
Map | rs4434423 |
PheGenI | rs4434423 |
Biobank | rs4434423 |
1000 genomes | rs4434423 |
hgdp | rs4434423 |
ensembl | rs4434423 |
geneview | rs4434423 |
scholar | rs4434423 |
rs4434423 | |
pharmgkb | rs4434423 |
gwascentral | rs4434423 |
openSNP | rs4434423 |
23andMe | rs4434423 |
SNPshot | rs4434423 |
SNPdbe | rs4434423 |
MSV3d | rs4434423 |
GWAS Ctlg | rs4434423 |
GMAF | 0.3985 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24467603] Genetic Variation in Prostaglandin E2 Pathway is Associated with Primary Graft Dysfunction