rs773499329
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CTGCCCACAGGCCAGG;CTGCCCACAGGCCAGG) | 0 | common in clinvar |
Make rs773499329(-;-) |
Make rs773499329(-;CTGCCCACAGGCCAGG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 97373561 |
Gene | DPYD, LOC105378867 |
is a | snp |
is | mentioned by |
dbSNP | rs773499329 |
dbSNP (classic) | rs773499329 |
ClinGen | rs773499329 |
ebi | rs773499329 |
HLI | rs773499329 |
Exac | rs773499329 |
Gnomad | rs773499329 |
Varsome | rs773499329 |
LitVar | rs773499329 |
Map | rs773499329 |
PheGenI | rs773499329 |
Biobank | rs773499329 |
1000 genomes | rs773499329 |
hgdp | rs773499329 |
ensembl | rs773499329 |
geneview | rs773499329 |
scholar | rs773499329 |
rs773499329 | |
pharmgkb | rs773499329 |
gwascentral | rs773499329 |
openSNP | rs773499329 |
23andMe | rs773499329 |
SNPshot | rs773499329 |
SNPdbe | rs773499329 |
MSV3d | rs773499329 |
GWAS Ctlg | rs773499329 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773499329(-;-) |
Alt | rs773499329(-;-) |
Reference | Rs773499329(CTGCCCACAGGCCAGG;CTGCCCACAGGCCAGG) |
Significance | Probable-Pathogenic |
Disease | Dihydropyrimidine dehydrogenase deficiency |
Variation | info |
Gene | DPYD |
CLNDBN | Dihydropyrimidine dehydrogenase deficiency |
Reversed | 0 |
HGVS | NC_000001.10:g.97839117_97839132del16 |
CLNSRC | |
CLNACC | RCV000169225.1, |