rs59086055
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs59086055(A;A) |
Make rs59086055(A;G) |
Make rs59086055(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 97450190 |
Gene | DPYD |
is a | snp |
is | mentioned by |
dbSNP | rs59086055 |
dbSNP (classic) | rs59086055 |
ClinGen | rs59086055 |
ebi | rs59086055 |
HLI | rs59086055 |
Exac | rs59086055 |
Gnomad | rs59086055 |
Varsome | rs59086055 |
LitVar | rs59086055 |
Map | rs59086055 |
PheGenI | rs59086055 |
Biobank | rs59086055 |
1000 genomes | rs59086055 |
hgdp | rs59086055 |
ensembl | rs59086055 |
geneview | rs59086055 |
scholar | rs59086055 |
rs59086055 | |
pharmgkb | rs59086055 |
gwascentral | rs59086055 |
openSNP | rs59086055 |
23andMe | rs59086055 |
SNPshot | rs59086055 |
SNPdbe | rs59086055 |
MSV3d | rs59086055 |
GWAS Ctlg | rs59086055 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs59086055(A;A) |
Alt | rs59086055(A;A) |
Reference | rs59086055(G;G) |
Significance | Unknown |
Disease | not specified |
Variation | info |
Gene | DPYD |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.97915746G>A |
CLNSRC | |
CLNACC | RCV000280781.1, |