rs1057516873
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1057516873(A;T) |
Make rs1057516873(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 97098575 |
Gene | DPYD, DPYD-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057516873 |
dbSNP (classic) | rs1057516873 |
ClinGen | rs1057516873 |
ebi | rs1057516873 |
HLI | rs1057516873 |
Exac | rs1057516873 |
Gnomad | rs1057516873 |
Varsome | rs1057516873 |
LitVar | rs1057516873 |
Map | rs1057516873 |
PheGenI | rs1057516873 |
Biobank | rs1057516873 |
1000 genomes | rs1057516873 |
hgdp | rs1057516873 |
ensembl | rs1057516873 |
geneview | rs1057516873 |
scholar | rs1057516873 |
rs1057516873 | |
pharmgkb | rs1057516873 |
gwascentral | rs1057516873 |
openSNP | rs1057516873 |
23andMe | rs1057516873 |
SNPshot | rs1057516873 |
SNPdbe | rs1057516873 |
MSV3d | rs1057516873 |
GWAS Ctlg | rs1057516873 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057516873(T;T) |
Alt | rs1057516873(T;T) |
Reference | Rs1057516873(A;A) |
Significance | Probable-Pathogenic |
Disease | Dihydropyrimidine dehydrogenase deficiency |
Variation | info |
Gene | DPYD-AS1 DPYD |
CLNDBN | Dihydropyrimidine dehydrogenase deficiency |
Reversed | 1 |
HGVS | NC_000001.10:g.97564131T>A |
CLNSRC | |
CLNACC | RCV000409198.1, |