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rs1053726

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1053726(C;C)
Make rs1053726(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354270
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1053726
ebirs1053726
HLIrs1053726
Exacrs1053726
Varsomers1053726
Maprs1053726
PheGenIrs1053726
hapmaprs1053726
1000 genomesrs1053726
hgdprs1053726
ensemblrs1053726
gopubmedrs1053726
geneviewrs1053726
scholarrs1053726
googlers1053726
pharmgkbrs1053726
gwascentralrs1053726
openSNPrs1053726
23andMers1053726
23andMe allrs1053726
SNP Nexus

SNPshotrs1053726
SNPdbers1053726
MSV3drs1053726
GWAS Ctlgrs1053726
GMAF0.1405
Max Magnitude0
ClinVar
Risk rs1053726(A,C;A,C)
Alt rs1053726(A,C;A,C)
Reference rs1053726(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322047A>G
CLNSRC
CLNACC