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rs1050240

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1050240(A;G)
Make rs1050240(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355357
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050240
dbSNP (classic)rs1050240
ClinGenrs1050240
ebirs1050240
HLIrs1050240
Exacrs1050240
Gnomadrs1050240
Varsomers1050240
LitVarrs1050240
Maprs1050240
PheGenIrs1050240
Biobankrs1050240
1000 genomesrs1050240
hgdprs1050240
ensemblrs1050240
geneviewrs1050240
scholarrs1050240
googlers1050240
pharmgkbrs1050240
gwascentralrs1050240
openSNPrs1050240
23andMers1050240
SNPshotrs1050240
SNPdbers1050240
MSV3drs1050240
GWAS Ctlgrs1050240
Max Magnitude0
ClinVar
Risk rs1050240(G;G) rs1050240(T;T)
Alt rs1050240(G;G) rs1050240(T;T)
Reference Rs1050240(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323134T>C
CLNSRC
CLNACC