rs369061090
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs369061090(A;A) |
Make rs369061090(A;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 210606897 |
Gene | CPS1 |
is a | snp |
is | mentioned by |
dbSNP | rs369061090 |
dbSNP (classic) | rs369061090 |
ClinGen | rs369061090 |
ebi | rs369061090 |
HLI | rs369061090 |
Exac | rs369061090 |
Gnomad | rs369061090 |
Varsome | rs369061090 |
LitVar | rs369061090 |
Map | rs369061090 |
PheGenI | rs369061090 |
Biobank | rs369061090 |
1000 genomes | rs369061090 |
hgdp | rs369061090 |
ensembl | rs369061090 |
geneview | rs369061090 |
scholar | rs369061090 |
rs369061090 | |
pharmgkb | rs369061090 |
gwascentral | rs369061090 |
openSNP | rs369061090 |
23andMe | rs369061090 |
SNPshot | rs369061090 |
SNPdbe | rs369061090 |
MSV3d | rs369061090 |
GWAS Ctlg | rs369061090 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369061090(A;A) |
Alt | rs369061090(A;A) |
Reference | Rs369061090(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CPS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.211471621T>A |
CLNSRC | |
CLNACC | RCV000344019.1, |