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rs2478545

From SNPedia

Orientationminus
Stabilizedminus
Make rs2478545(C;C)
Make rs2478545(C;T)
Make rs2478545(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position230708375
GeneAGT
is asnp
is mentioned by
dbSNPrs2478545
dbSNP (classic)rs2478545
ClinGenrs2478545
ebirs2478545
HLIrs2478545
Exacrs2478545
Gnomadrs2478545
Varsomers2478545
LitVarrs2478545
Maprs2478545
PheGenIrs2478545
Biobankrs2478545
1000 genomesrs2478545
hgdprs2478545
ensemblrs2478545
geneviewrs2478545
scholarrs2478545
googlers2478545
pharmgkbrs2478545
gwascentralrs2478545
openSNPrs2478545
23andMers2478545
SNPshotrs2478545
SNPdbers2478545
MSV3drs2478545
GWAS Ctlgrs2478545
GMAF0.3411
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22739771] Genetic variation in the renin-angiotensin-aldosterone system is associated with cardiovascular risk factors and early mortality in established coronary heart disease


[PMID 19064790OA-icon.png] Predictive genomics of cardioembolic stroke.


[PMID 19105203OA-icon.png] An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.


[PMID 20537141OA-icon.png] Maternal angiotensinogen (AGT) haplotypes, fetal renin (REN) haplotypes and risk of preeclampsia; estimation of gene-gene interaction from family-triad data.