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rs1055348

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1055348(A;C)
Make rs1055348(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354171
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1055348
ebirs1055348
HLIrs1055348
Exacrs1055348
Varsomers1055348
Maprs1055348
PheGenIrs1055348
hapmaprs1055348
1000 genomesrs1055348
hgdprs1055348
ensemblrs1055348
gopubmedrs1055348
geneviewrs1055348
scholarrs1055348
googlers1055348
pharmgkbrs1055348
gwascentralrs1055348
openSNPrs1055348
23andMers1055348
23andMe allrs1055348
SNP Nexus

SNPshotrs1055348
SNPdbers1055348
MSV3drs1055348
GWAS Ctlgrs1055348
GMAF0.1758
Max Magnitude0
ClinVar
Risk rs1055348(C;C)
Alt rs1055348(C;C)
Reference rs1055348(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31321948T>G
CLNSRC
CLNACC