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rs1050458

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1050458(C;C)
Make rs1050458(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357148
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050458
dbSNP (classic)rs1050458
ClinGenrs1050458
ebirs1050458
HLIrs1050458
Exacrs1050458
Gnomadrs1050458
Varsomers1050458
LitVarrs1050458
Maprs1050458
PheGenIrs1050458
Biobankrs1050458
1000 genomesrs1050458
hgdprs1050458
ensemblrs1050458
geneviewrs1050458
scholarrs1050458
googlers1050458
pharmgkbrs1050458
gwascentralrs1050458
openSNPrs1050458
23andMers1050458
SNPshotrs1050458
SNPdbers1050458
MSV3drs1050458
GWAS Ctlgrs1050458
GMAF0.264
Max Magnitude0
ClinVar
Risk rs1050458(C;C) rs1050458(G;G)
Alt rs1050458(C;C) rs1050458(G;G)
Reference Rs1050458(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324925A>G
CLNSRC
CLNACC