rs778806374
From SNPedia
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 |
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, |