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rs144012689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs144012689(A;A)
Make rs144012689(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355003
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs144012689
dbSNP (classic)rs144012689
ClinGenrs144012689
ebirs144012689
HLIrs144012689
Exacrs144012689
Gnomadrs144012689
Varsomers144012689
LitVarrs144012689
Maprs144012689
PheGenIrs144012689
Biobankrs144012689
1000 genomesrs144012689
hgdprs144012689
ensemblrs144012689
geneviewrs144012689
scholarrs144012689
googlers144012689
pharmgkbrs144012689
gwascentralrs144012689
openSNPrs144012689
23andMers144012689
SNPshotrs144012689
SNPdbers144012689
MSV3drs144012689
GWAS Ctlgrs144012689
GMAF0.00551
Max Magnitude0
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 30971914OA-icon.png] A Screening Test for HLA-B∗15:02 in a Large United States Patient Cohort Identifies Broader Risk of Carbamazepine-Induced Adverse Events.