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rs2308466

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2308466(A;T)
Make rs2308466(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356226
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2308466
ebirs2308466
HLIrs2308466
Exacrs2308466
Varsomers2308466
Maprs2308466
PheGenIrs2308466
hapmaprs2308466
1000 genomesrs2308466
hgdprs2308466
ensemblrs2308466
gopubmedrs2308466
geneviewrs2308466
scholarrs2308466
googlers2308466
pharmgkbrs2308466
gwascentralrs2308466
openSNPrs2308466
23andMers2308466
23andMe allrs2308466
SNP Nexus

SNPshotrs2308466
SNPdbers2308466
MSV3drs2308466
GWAS Ctlgrs2308466
Max Magnitude0
ClinVar
Risk rs2308466(C,G,T;C,G,T)
Alt rs2308466(C,G,T;C,G,T)
Reference rs2308466(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324003T>A; NC_000006.11:g.31324003T>C; NC_000006.11:g.31324003T>G
CLNSRC
CLNACC