rs778806374

Orientation

plus

Stabilized

plus

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

Make rs778806374(A;A)

Make rs778806374(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

230705970

Gene

AGT

is a	snp
is	mentioned by
dbSNP	rs778806374
dbSNP (classic)	rs778806374
ClinGen	rs778806374
ebi	rs778806374
HLI	rs778806374
Exac	rs778806374
Gnomad	rs778806374
Varsome	rs778806374
LitVar	rs778806374
Map	rs778806374
PheGenI	rs778806374
Biobank	rs778806374
1000 genomes	rs778806374
hgdp	rs778806374
ensembl	rs778806374
geneview	rs778806374
scholar	rs778806374
google	rs778806374
pharmgkb	rs778806374
gwascentral	rs778806374
openSNP	rs778806374
23andMe	rs778806374
SNPshot	rs778806374
SNPdbe	rs778806374
MSV3d	rs778806374
GWAS Ctlg	rs778806374

Max Magnitude

0

ClinVar
Risk	rs778806374(A;A)
Alt	rs778806374(A;A)
Reference	Rs778806374(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	AGT
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.230841716G>A
CLNSRC
CLNACC	RCV000492929.1,