rs771053807
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs771053807(-;CAGTTC) |
Make rs771053807(CAGTTC;CAGTTC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 63483870 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs771053807 |
dbSNP (classic) | rs771053807 |
ClinGen | rs771053807 |
ebi | rs771053807 |
HLI | rs771053807 |
Exac | rs771053807 |
Gnomad | rs771053807 |
Varsome | rs771053807 |
LitVar | rs771053807 |
Map | rs771053807 |
PheGenI | rs771053807 |
Biobank | rs771053807 |
1000 genomes | rs771053807 |
hgdp | rs771053807 |
ensembl | rs771053807 |
geneview | rs771053807 |
scholar | rs771053807 |
rs771053807 | |
pharmgkb | rs771053807 |
gwascentral | rs771053807 |
openSNP | rs771053807 |
23andMe | rs771053807 |
SNPshot | rs771053807 |
SNPdbe | rs771053807 |
MSV3d | rs771053807 |
GWAS Ctlg | rs771053807 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs771053807(CAGTTC;CAGTTC) |
Alt | rs771053807(CAGTTC;CAGTTC) |
Reference | Rs771053807(-;-) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.61561231_61561232insCAGTTC |
CLNSRC | |
CLNACC | RCV000224410.1, |