rs115232898
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs115232898(C;C) |
Make rs115232898(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 97699474 |
Gene | DPYD |
is a | snp |
is | mentioned by |
dbSNP | rs115232898 |
dbSNP (classic) | rs115232898 |
ClinGen | rs115232898 |
ebi | rs115232898 |
HLI | rs115232898 |
Exac | rs115232898 |
Gnomad | rs115232898 |
Varsome | rs115232898 |
LitVar | rs115232898 |
Map | rs115232898 |
PheGenI | rs115232898 |
Biobank | rs115232898 |
1000 genomes | rs115232898 |
hgdp | rs115232898 |
ensembl | rs115232898 |
geneview | rs115232898 |
scholar | rs115232898 |
rs115232898 | |
pharmgkb | rs115232898 |
gwascentral | rs115232898 |
openSNP | rs115232898 |
23andMe | rs115232898 |
SNPshot | rs115232898 |
SNPdbe | rs115232898 |
MSV3d | rs115232898 |
GWAS Ctlg | rs115232898 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs115232898(C;C) |
Alt | rs115232898(C;C) |
Reference | Rs115232898(T;T) |
Significance | Untested |
Disease | not provided |
Variation | info |
Gene | DPYD |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.98165030T>C |
CLNSRC | ClinVar |
CLNACC | RCV000086496.1, |