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rs1050823

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1050823(C;C)
Make rs1050823(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355426
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050823
dbSNP (classic)rs1050823
ClinGenrs1050823
ebirs1050823
HLIrs1050823
Exacrs1050823
Gnomadrs1050823
Varsomers1050823
LitVarrs1050823
Maprs1050823
PheGenIrs1050823
Biobankrs1050823
1000 genomesrs1050823
hgdprs1050823
ensemblrs1050823
geneviewrs1050823
scholarrs1050823
googlers1050823
pharmgkbrs1050823
gwascentralrs1050823
openSNPrs1050823
23andMers1050823
SNPshotrs1050823
SNPdbers1050823
MSV3drs1050823
GWAS Ctlgrs1050823
GMAF0.07346
Max Magnitude0
ClinVar
Risk rs1050823(C;C)
Alt rs1050823(C;C)
Reference Rs1050823(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323203A>G
CLNSRC
CLNACC