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rs2276448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2276448(A;G)
Make rs2276448(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355243
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2276448
ebirs2276448
HLIrs2276448
Exacrs2276448
Varsomers2276448
Maprs2276448
PheGenIrs2276448
hapmaprs2276448
1000 genomesrs2276448
hgdprs2276448
ensemblrs2276448
gopubmedrs2276448
geneviewrs2276448
scholarrs2276448
googlers2276448
pharmgkbrs2276448
gwascentralrs2276448
openSNPrs2276448
23andMers2276448
23andMe allrs2276448
SNP Nexus

SNPshotrs2276448
SNPdbers2276448
MSV3drs2276448
GWAS Ctlgrs2276448
GMAF0.2911
Max Magnitude0
ClinVar
Risk rs2276448(C,G,T;C,G,T)
Alt rs2276448(C,G,T;C,G,T)
Reference rs2276448(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323020T>C
CLNSRC
CLNACC