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rs138659308

From SNPedia

Merged intors1131201
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs138659308(C;C)
Make rs138659308(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356765
GeneHLA-B
is asnp
is mentioned by
dbSNPrs138659308
ebirs138659308
HLIrs138659308
Exacrs138659308
Varsomers138659308
Maprs138659308
PheGenIrs138659308
hapmaprs138659308
1000 genomesrs138659308
hgdprs138659308
ensemblrs138659308
gopubmedrs138659308
geneviewrs138659308
scholarrs138659308
googlers138659308
pharmgkbrs138659308
gwascentralrs138659308
openSNPrs138659308
23andMers138659308
23andMe allrs138659308
SNP Nexus

SNPshotrs138659308
SNPdbers138659308
MSV3drs138659308
GWAS Ctlgrs138659308
StatusMerged into rs1131201
Max Magnitude0
ClinVar
Risk rs138659308(C;C)
Alt rs138659308(C;C)
Reference rs138659308(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324542T>C
CLNSRC
CLNACC