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rs1051488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1051488(A;A)
Make rs1051488(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355134
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1051488
dbSNP (classic)rs1051488
ClinGenrs1051488
ebirs1051488
HLIrs1051488
Exacrs1051488
Gnomadrs1051488
Varsomers1051488
LitVarrs1051488
Maprs1051488
PheGenIrs1051488
Biobankrs1051488
1000 genomesrs1051488
hgdprs1051488
ensemblrs1051488
geneviewrs1051488
scholarrs1051488
googlers1051488
pharmgkbrs1051488
gwascentralrs1051488
openSNPrs1051488
23andMers1051488
SNPshotrs1051488
SNPdbers1051488
MSV3drs1051488
GWAS Ctlgrs1051488
GMAF0.4725
Max Magnitude0
ClinVar
Risk rs1051488(A;A) rs1051488(C;C)
Alt rs1051488(A;A) rs1051488(C;C)
Reference Rs1051488(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322911C>T
CLNSRC
CLNACC