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rs4869419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs4869419(A;G)
Make rs4869419(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position93231833
is asnp
is mentioned by
dbSNPrs4869419
ebirs4869419
HLIrs4869419
Exacrs4869419
Varsomers4869419
Maprs4869419
PheGenIrs4869419
hapmaprs4869419
1000 genomesrs4869419
hgdprs4869419
ensemblrs4869419
gopubmedrs4869419
geneviewrs4869419
scholarrs4869419
googlers4869419
pharmgkbrs4869419
gwascentralrs4869419
openSNPrs4869419
23andMers4869419
23andMe allrs4869419
SNP Nexus

SNPshotrs4869419
SNPdbers4869419
MSV3drs4869419
GWAS Ctlgrs4869419
GMAF0.07805
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21273288OA-icon.png]
Trait
Title Genome-Wide Association Analysis and Fine Mapping of NT-proBNP Level Provide Novel Insight into the Role of the MTHFR-CLCN6-NPPA-NPPB Gene Cluster
Risk Allele G
P-val 0.000004
Odds Ratio 0.2000 [0.12-0.28] unit decrease