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rs144295468

From SNPedia

Orientationplus
Stabilizedplus
Make rs144295468(A;A)
Make rs144295468(A;G)
Make rs144295468(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31363122
is asnp
is mentioned by
dbSNPrs144295468
dbSNP (classic)rs144295468
ClinGenrs144295468
ebirs144295468
HLIrs144295468
Exacrs144295468
Gnomadrs144295468
Varsomers144295468
LitVarrs144295468
Maprs144295468
PheGenIrs144295468
Biobankrs144295468
1000 genomesrs144295468
hgdprs144295468
ensemblrs144295468
geneviewrs144295468
scholarrs144295468
googlers144295468
pharmgkbrs144295468
gwascentralrs144295468
openSNPrs144295468
23andMers144295468
23andMe allrs144295468
SNPshotrs144295468
SNPdbers144295468
MSV3drs144295468
GWAS Ctlgrs144295468
Max Magnitude

[PMID 28398356] SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.