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rs1055890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1055890(C;C)
Make rs1055890(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354138
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1055890
ebirs1055890
HLIrs1055890
Exacrs1055890
Varsomers1055890
Maprs1055890
PheGenIrs1055890
hapmaprs1055890
1000 genomesrs1055890
hgdprs1055890
ensemblrs1055890
gopubmedrs1055890
geneviewrs1055890
scholarrs1055890
googlers1055890
pharmgkbrs1055890
gwascentralrs1055890
openSNPrs1055890
23andMers1055890
23andMe allrs1055890
SNP Nexus

SNPshotrs1055890
SNPdbers1055890
MSV3drs1055890
GWAS Ctlgrs1055890
GMAF0.2828
Max Magnitude0
ClinVar
Risk rs1055890(C;C)
Alt rs1055890(C;C)
Reference rs1055890(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31321915A>G
CLNSRC
CLNACC