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rs1918974

From SNPedia

Orientationplus
Stabilizedplus
Make rs1918974(C;C)
Make rs1918974(C;T)
Make rs1918974(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position169448100
GeneMECOM
is asnp
is mentioned by
dbSNPrs1918974
ebirs1918974
HLIrs1918974
Exacrs1918974
Varsomers1918974
Maprs1918974
PheGenIrs1918974
hapmaprs1918974
1000 genomesrs1918974
hgdprs1918974
ensemblrs1918974
gopubmedrs1918974
geneviewrs1918974
scholarrs1918974
googlers1918974
pharmgkbrs1918974
gwascentralrs1918974
openSNPrs1918974
23andMers1918974
23andMe allrs1918974
SNP Nexus

SNPshotrs1918974
SNPdbers1918974
MSV3drs1918974
GWAS Ctlgrs1918974
GMAF0.3632
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19430483OA-icon.png]
Trait Diastolic Blood Pressure
Title Genome-wide association study identifies eight loci associated with blood pressure
Risk Allele T
P-val 8E-8
Odds Ratio 0.27 [0.17-0.37] mm Hg decrease


GET Evidence
rs1918974
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.59375
summary