rs367797185
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs367797185(C;T) |
Make rs367797185(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 63483494 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs367797185 |
dbSNP (classic) | rs367797185 |
ClinGen | rs367797185 |
ebi | rs367797185 |
HLI | rs367797185 |
Exac | rs367797185 |
Gnomad | rs367797185 |
Varsome | rs367797185 |
LitVar | rs367797185 |
Map | rs367797185 |
PheGenI | rs367797185 |
Biobank | rs367797185 |
1000 genomes | rs367797185 |
hgdp | rs367797185 |
ensembl | rs367797185 |
geneview | rs367797185 |
scholar | rs367797185 |
rs367797185 | |
pharmgkb | rs367797185 |
gwascentral | rs367797185 |
openSNP | rs367797185 |
23andMe | rs367797185 |
SNPshot | rs367797185 |
SNPdbe | rs367797185 |
MSV3d | rs367797185 |
GWAS Ctlg | rs367797185 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs367797185(T;T) |
Alt | rs367797185(T;T) |
Reference | Rs367797185(C;C) |
Significance | Pathogenic |
Disease | not provided Renal dysplasia |
Variation | info |
Gene | ACE |
CLNDBN | not provided Renal dysplasia |
Reversed | 0 |
HGVS | NC_000017.10:g.61560855C>T |
CLNSRC | |
CLNACC | RCV000224863.1, RCV000399495.1, |