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rs4434423

From SNPedia

Orientationplus
Stabilizedplus
Make rs4434423(A;A)
Make rs4434423(A;T)
Make rs4434423(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position40677580
is asnp
is mentioned by
dbSNPrs4434423
ebirs4434423
HLIrs4434423
Exacrs4434423
Varsomers4434423
Maprs4434423
PheGenIrs4434423
hapmaprs4434423
1000 genomesrs4434423
hgdprs4434423
ensemblrs4434423
gopubmedrs4434423
geneviewrs4434423
scholarrs4434423
googlers4434423
pharmgkbrs4434423
gwascentralrs4434423
openSNPrs4434423
23andMers4434423
23andMe allrs4434423
SNP Nexus

SNPshotrs4434423
SNPdbers4434423
MSV3drs4434423
GWAS Ctlgrs4434423
GMAF0.3985
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 24467603OA-icon.png] Genetic Variation in Prostaglandin E2 Pathway is Associated with Primary Graft Dysfunction