rs779422412
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs779422412(C;T) |
Make rs779422412(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 63478093 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs779422412 |
dbSNP (classic) | rs779422412 |
ClinGen | rs779422412 |
ebi | rs779422412 |
HLI | rs779422412 |
Exac | rs779422412 |
Gnomad | rs779422412 |
Varsome | rs779422412 |
LitVar | rs779422412 |
Map | rs779422412 |
PheGenI | rs779422412 |
Biobank | rs779422412 |
1000 genomes | rs779422412 |
hgdp | rs779422412 |
ensembl | rs779422412 |
geneview | rs779422412 |
scholar | rs779422412 |
rs779422412 | |
pharmgkb | rs779422412 |
gwascentral | rs779422412 |
openSNP | rs779422412 |
23andMe | rs779422412 |
SNPshot | rs779422412 |
SNPdbe | rs779422412 |
MSV3d | rs779422412 |
GWAS Ctlg | rs779422412 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs779422412(T;T) |
Alt | rs779422412(T;T) |
Reference | Rs779422412(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.61555454C>T |
CLNSRC | |
CLNACC | RCV000481663.1, |