rs747815674

Orientation

plus

Stabilized

plus

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

Make rs747815674(A;A)

Make rs747815674(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

230709994

Gene

AGT

is a	snp
is	mentioned by
dbSNP	rs747815674
dbSNP (classic)	rs747815674
ClinGen	rs747815674
ebi	rs747815674
HLI	rs747815674
Exac	rs747815674
Gnomad	rs747815674
Varsome	rs747815674
LitVar	rs747815674
Map	rs747815674
PheGenI	rs747815674
Biobank	rs747815674
1000 genomes	rs747815674
hgdp	rs747815674
ensembl	rs747815674
geneview	rs747815674
scholar	rs747815674
google	rs747815674
pharmgkb	rs747815674
gwascentral	rs747815674
openSNP	rs747815674
23andMe	rs747815674
SNPshot	rs747815674
SNPdbe	rs747815674
MSV3d	rs747815674
GWAS Ctlg	rs747815674

Max Magnitude

0

ClinVar
Risk	rs747815674(A;A)
Alt	rs747815674(A;A)
Reference	Rs747815674(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	AGT
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.230845740C>A
CLNSRC
CLNACC	RCV000493969.1,