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rs2308488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2308488(A;A)
Make rs2308488(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355407
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2308488
ebirs2308488
HLIrs2308488
Exacrs2308488
Varsomers2308488
Maprs2308488
PheGenIrs2308488
hapmaprs2308488
1000 genomesrs2308488
hgdprs2308488
ensemblrs2308488
gopubmedrs2308488
geneviewrs2308488
scholarrs2308488
googlers2308488
pharmgkbrs2308488
gwascentralrs2308488
openSNPrs2308488
23andMers2308488
23andMe allrs2308488
SNP Nexus

SNPshotrs2308488
SNPdbers2308488
MSV3drs2308488
GWAS Ctlgrs2308488
GMAF0.02112
Max Magnitude0
ClinVar
Risk rs2308488(A,C,T;A,C,T)
Alt rs2308488(A,C,T;A,C,T)
Reference rs2308488(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323184C>T
CLNSRC
CLNACC