rs778390161
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs778390161(A;A) |
Make rs778390161(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 63490953 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs778390161 |
dbSNP (classic) | rs778390161 |
ClinGen | rs778390161 |
ebi | rs778390161 |
HLI | rs778390161 |
Exac | rs778390161 |
Gnomad | rs778390161 |
Varsome | rs778390161 |
LitVar | rs778390161 |
Map | rs778390161 |
PheGenI | rs778390161 |
Biobank | rs778390161 |
1000 genomes | rs778390161 |
hgdp | rs778390161 |
ensembl | rs778390161 |
geneview | rs778390161 |
scholar | rs778390161 |
rs778390161 | |
pharmgkb | rs778390161 |
gwascentral | rs778390161 |
openSNP | rs778390161 |
23andMe | rs778390161 |
SNPshot | rs778390161 |
SNPdbe | rs778390161 |
MSV3d | rs778390161 |
GWAS Ctlg | rs778390161 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs778390161(A;A) |
Alt | rs778390161(A;A) |
Reference | Rs778390161(G;G) |
Significance | Probable-Pathogenic |
Disease | Renal dysplasia |
Variation | info |
Gene | ACE |
CLNDBN | Renal dysplasia |
Reversed | 0 |
HGVS | NC_000017.10:g.61568314G>A |
CLNSRC | |
CLNACC | RCV000416335.1, |