rs199476082

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs199476082(A;T)

Make rs199476082(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

230710823

Gene

AGT

is a	snp
is	mentioned by
dbSNP	rs199476082
dbSNP (classic)	rs199476082
ClinGen	rs199476082
ebi	rs199476082
HLI	rs199476082
Exac	rs199476082
Gnomad	rs199476082
Varsome	rs199476082
LitVar	rs199476082
Map	rs199476082
PheGenI	rs199476082
Biobank	rs199476082
1000 genomes	rs199476082
hgdp	rs199476082
ensembl	rs199476082
geneview	rs199476082
scholar	rs199476082
google	rs199476082
pharmgkb	rs199476082
gwascentral	rs199476082
openSNP	rs199476082
23andMe	rs199476082
SNPshot	rs199476082
SNPdbe	rs199476082
MSV3d	rs199476082
GWAS Ctlg	rs199476082

Max Magnitude

0

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