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rs1050628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1050628(C;C)
Make rs1050628(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356375
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050628
dbSNP (classic)rs1050628
ClinGenrs1050628
ebirs1050628
HLIrs1050628
Exacrs1050628
Gnomadrs1050628
Varsomers1050628
LitVarrs1050628
Maprs1050628
PheGenIrs1050628
Biobankrs1050628
1000 genomesrs1050628
hgdprs1050628
ensemblrs1050628
geneviewrs1050628
scholarrs1050628
googlers1050628
pharmgkbrs1050628
gwascentralrs1050628
openSNPrs1050628
23andMers1050628
SNPshotrs1050628
SNPdbers1050628
MSV3drs1050628
GWAS Ctlgrs1050628
Max Magnitude0
ClinVar
Risk rs1050628(C;C)
Alt rs1050628(C;C)
Reference Rs1050628(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324152A>G
CLNSRC
CLNACC