Have questions? Visit https://www.reddit.com/r/SNPedia

rs1050654

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050654(A;A)
Make rs1050654(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356323
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050654
dbSNP (classic)rs1050654
ClinGenrs1050654
ebirs1050654
HLIrs1050654
Exacrs1050654
Gnomadrs1050654
Varsomers1050654
LitVarrs1050654
Maprs1050654
PheGenIrs1050654
Biobankrs1050654
1000 genomesrs1050654
hgdprs1050654
ensemblrs1050654
geneviewrs1050654
scholarrs1050654
googlers1050654
pharmgkbrs1050654
gwascentralrs1050654
openSNPrs1050654
23andMers1050654
SNPshotrs1050654
SNPdbers1050654
MSV3drs1050654
GWAS Ctlgrs1050654
GMAF0.4201
Max Magnitude0
ClinVar
Risk rs1050654(A;A) rs1050654(T;T)
Alt rs1050654(A;A) rs1050654(T;T)
Reference Rs1050654(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324100G>A; NC_000006.11:g.31324100G>T
CLNSRC
CLNACC