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rs12946454

From SNPedia

Orientationplus
Stabilizedplus
Make rs12946454(A;A)
Make rs12946454(A;T)
Make rs12946454(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position45130754
GeneACBD4, PLCD3
is asnp
is mentioned by
dbSNPrs12946454
ebirs12946454
HLIrs12946454
Exacrs12946454
Varsomers12946454
Maprs12946454
PheGenIrs12946454
hapmaprs12946454
1000 genomesrs12946454
hgdprs12946454
ensemblrs12946454
gopubmedrs12946454
geneviewrs12946454
scholarrs12946454
googlers12946454
pharmgkbrs12946454
gwascentralrs12946454
openSNPrs12946454
23andMers12946454
23andMe allrs12946454
SNP Nexus

SNPshotrs12946454
SNPdbers12946454
MSV3drs12946454
GWAS Ctlgrs12946454
GMAF0.2057
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 19430483OA-icon.png]

23andMe blog blood pressure

GWAS snp
PMID [PMID 19430483OA-icon.png]
Trait Systolic blood pressure
Title Genome-wide association study identifies eight loci associated with blood pressure
Risk Allele T
P-val 1E-8
Odds Ratio 0.57 [0.37-0.77] mm Hg increase


[PMID 22525200] Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.


GET Evidence
rs12946454
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary