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rs199476082

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199476082(A;T)
Make rs199476082(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position230710823
GeneAGT
is asnp
is mentioned by
dbSNPrs199476082
ebirs199476082
HLIrs199476082
Exacrs199476082
Varsomers199476082
Maprs199476082
PheGenIrs199476082
hapmaprs199476082
1000 genomesrs199476082
hgdprs199476082
ensemblrs199476082
gopubmedrs199476082
geneviewrs199476082
scholarrs199476082
googlers199476082
pharmgkbrs199476082
gwascentralrs199476082
openSNPrs199476082
23andMers199476082
23andMe allrs199476082
SNP Nexus

SNPshotrs199476082
SNPdbers199476082
MSV3drs199476082
GWAS Ctlgrs199476082
Max Magnitude0
ClinVar
Risk rs199476082(T;T)
Alt rs199476082(T;T)
Reference rs199476082(A;A)
Significance Probable-Pathogenic
Disease Essential hypertension
Variation info
Gene AGT
CLNDBN Essential hypertension
Reversed 1
HGVS NC_000001.10:g.230846569T>A
CLNSRC
CLNACC