rs186364861
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs186364861(A;A) |
Make rs186364861(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 13 |
Position | 48037798 |
Gene | NUDT15, SUCLA2 |
is a | snp |
is | mentioned by |
dbSNP | rs186364861 |
dbSNP (classic) | rs186364861 |
ClinGen | rs186364861 |
ebi | rs186364861 |
HLI | rs186364861 |
Exac | rs186364861 |
Gnomad | rs186364861 |
Varsome | rs186364861 |
LitVar | rs186364861 |
Map | rs186364861 |
PheGenI | rs186364861 |
Biobank | rs186364861 |
1000 genomes | rs186364861 |
hgdp | rs186364861 |
ensembl | rs186364861 |
geneview | rs186364861 |
scholar | rs186364861 |
rs186364861 | |
pharmgkb | rs186364861 |
gwascentral | rs186364861 |
openSNP | rs186364861 |
23andMe | rs186364861 |
SNPshot | rs186364861 |
SNPdbe | rs186364861 |
MSV3d | rs186364861 |
GWAS Ctlg | rs186364861 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs186364861(A;A) |
Alt | rs186364861(A;A) |
Reference | Rs186364861(G;G) |
Significance | Drug-response |
Disease | Thiopurines |
Variation | info |
Gene | NUDT15 SUCLA2 |
CLNDBN | Thiopurines, poor metabolism of, 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.48611934G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000210850.1, |