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rs448378

From SNPedia

Orientationplus
Stabilizedplus
Make rs448378(A;A)
Make rs448378(A;G)
Make rs448378(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position169383111
GeneMECOM
is asnp
is mentioned by
dbSNPrs448378
ebirs448378
HLIrs448378
Exacrs448378
Varsomers448378
Maprs448378
PheGenIrs448378
hapmaprs448378
1000 genomesrs448378
hgdprs448378
ensemblrs448378
gopubmedrs448378
geneviewrs448378
scholarrs448378
googlers448378
pharmgkbrs448378
gwascentralrs448378
openSNPrs448378
23andMers448378
23andMe allrs448378
SNP Nexus

SNPshotrs448378
SNPdbers448378
MSV3drs448378
GWAS Ctlgrs448378
GMAF0.416
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19430479OA-icon.png]
Trait Systolic blood pressure
Title Genome-wide association study of blood pressure and hypertension
Risk Allele A
P-val 1E-7
Odds Ratio 0.51 [0.31-0.71] mm Hg decrease
GWAS snp
PMID [PMID 20700443OA-icon.png]
Trait
Title Genome-Wide Association Studies of Serum Magnesium, Potassium, and Sodium Concentrations Identify Six Loci Influencing Serum Magnesium Levels
Risk Allele G
P-val 1E-8
Odds Ratio 0 [0.002-0.006] mmol/L decrease


GET Evidence
rs448378
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.546875
summary