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rs1050723

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050723(C;T)
Make rs1050723(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355544
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050723
dbSNP (old)rs1050723
ClinGenrs1050723
ebirs1050723
HLIrs1050723
Exacrs1050723
Gnomadrs1050723
Varsomers1050723
Maprs1050723
PheGenIrs1050723
Biobankrs1050723
1000 genomesrs1050723
hgdprs1050723
ensemblrs1050723
gopubmedrs1050723
geneviewrs1050723
scholarrs1050723
googlers1050723
pharmgkbrs1050723
gwascentralrs1050723
openSNPrs1050723
23andMers1050723
23andMe allrs1050723
SNP Nexus

SNPshotrs1050723
SNPdbers1050723
MSV3drs1050723
GWAS Ctlgrs1050723
GMAF0.0877
Max Magnitude0
ClinVar
Risk rs1050723(T;T)
Alt rs1050723(T;T)
Reference Rs1050723(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323321G>A
CLNSRC
CLNACC