rs144012689
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs144012689(A;A) |
Make rs144012689(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31355003 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs144012689 |
dbSNP (classic) | rs144012689 |
ClinGen | rs144012689 |
ebi | rs144012689 |
HLI | rs144012689 |
Exac | rs144012689 |
Gnomad | rs144012689 |
Varsome | rs144012689 |
LitVar | rs144012689 |
Map | rs144012689 |
PheGenI | rs144012689 |
Biobank | rs144012689 |
1000 genomes | rs144012689 |
hgdp | rs144012689 |
ensembl | rs144012689 |
geneview | rs144012689 |
scholar | rs144012689 |
rs144012689 | |
pharmgkb | rs144012689 |
gwascentral | rs144012689 |
openSNP | rs144012689 |
23andMe | rs144012689 |
SNPshot | rs144012689 |
SNPdbe | rs144012689 |
MSV3d | rs144012689 |
GWAS Ctlg | rs144012689 |
GMAF | 0.00551 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs144012689(A;A) |
Alt | rs144012689(A;A) |
Reference | Rs144012689(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31322780T>A |
CLNSRC | |
CLNACC |
[PMID 28398356] SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.
[PMID 30971914] A Screening Test for HLA-B∗15:02 in a Large United States Patient Cohort Identifies Broader Risk of Carbamazepine-Induced Adverse Events.