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rs778806374

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778806374(A;A)
Make rs778806374(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position230705970
GeneAGT
is asnp
is mentioned by
dbSNPrs778806374
dbSNP (classic)rs778806374
ClinGenrs778806374
ebirs778806374
HLIrs778806374
Exacrs778806374
Gnomadrs778806374
Varsomers778806374
LitVarrs778806374
Maprs778806374
PheGenIrs778806374
Biobankrs778806374
1000 genomesrs778806374
hgdprs778806374
ensemblrs778806374
geneviewrs778806374
scholarrs778806374
googlers778806374
pharmgkbrs778806374
gwascentralrs778806374
openSNPrs778806374
23andMers778806374
23andMe allrs778806374
SNPshotrs778806374
SNPdbers778806374
MSV3drs778806374
GWAS Ctlgrs778806374
Max Magnitude0
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,