rs189768576
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs189768576(A;A) |
Make rs189768576(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 97828127 |
Gene | DPYD |
is a | snp |
is | mentioned by |
dbSNP | rs189768576 |
dbSNP (classic) | rs189768576 |
ClinGen | rs189768576 |
ebi | rs189768576 |
HLI | rs189768576 |
Exac | rs189768576 |
Gnomad | rs189768576 |
Varsome | rs189768576 |
LitVar | rs189768576 |
Map | rs189768576 |
PheGenI | rs189768576 |
Biobank | rs189768576 |
1000 genomes | rs189768576 |
hgdp | rs189768576 |
ensembl | rs189768576 |
geneview | rs189768576 |
scholar | rs189768576 |
rs189768576 | |
pharmgkb | rs189768576 |
gwascentral | rs189768576 |
openSNP | rs189768576 |
23andMe | rs189768576 |
SNPshot | rs189768576 |
SNPdbe | rs189768576 |
MSV3d | rs189768576 |
GWAS Ctlg | rs189768576 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs189768576(A;A) |
Alt | rs189768576(A;A) |
Reference | Rs189768576(G;G) |
Significance | Probable-Pathogenic |
Disease | Dihydropyrimidine dehydrogenase deficiency |
Variation | info |
Gene | DPYD |
CLNDBN | Dihydropyrimidine dehydrogenase deficiency |
Reversed | 0 |
HGVS | NC_000001.10:g.98293683G>A |
CLNSRC | |
CLNACC | RCV000411323.1, |