rs761345398
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs761345398(A;A) |
Make rs761345398(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 63483173 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs761345398 |
dbSNP (classic) | rs761345398 |
ClinGen | rs761345398 |
ebi | rs761345398 |
HLI | rs761345398 |
Exac | rs761345398 |
Gnomad | rs761345398 |
Varsome | rs761345398 |
LitVar | rs761345398 |
Map | rs761345398 |
PheGenI | rs761345398 |
Biobank | rs761345398 |
1000 genomes | rs761345398 |
hgdp | rs761345398 |
ensembl | rs761345398 |
geneview | rs761345398 |
scholar | rs761345398 |
rs761345398 | |
pharmgkb | rs761345398 |
gwascentral | rs761345398 |
openSNP | rs761345398 |
23andMe | rs761345398 |
SNPshot | rs761345398 |
SNPdbe | rs761345398 |
MSV3d | rs761345398 |
GWAS Ctlg | rs761345398 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761345398(A;A) |
Alt | rs761345398(A;A) |
Reference | Rs761345398(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.61560534G>A |
CLNSRC | |
CLNACC | RCV000479383.1, |