Have questions? Visit https://www.reddit.com/r/SNPedia

rs1055821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1055821(A;A)
Make rs1055821(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354142
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1055821
ebirs1055821
HLIrs1055821
Exacrs1055821
Varsomers1055821
Maprs1055821
PheGenIrs1055821
hapmaprs1055821
1000 genomesrs1055821
hgdprs1055821
ensemblrs1055821
gopubmedrs1055821
geneviewrs1055821
scholarrs1055821
googlers1055821
pharmgkbrs1055821
gwascentralrs1055821
openSNPrs1055821
23andMers1055821
23andMe allrs1055821
SNP Nexus

SNPshotrs1055821
SNPdbers1055821
MSV3drs1055821
GWAS Ctlgrs1055821
GMAF0.06474
Max Magnitude0
ClinVar
Risk rs1055821(A;A)
Alt rs1055821(A;A)
Reference rs1055821(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31321919G>T
CLNSRC
CLNACC