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rs17881233

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17881233(G;T)
Make rs17881233(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355968
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs17881233
dbSNP (classic)rs17881233
ClinGenrs17881233
ebirs17881233
HLIrs17881233
Exacrs17881233
Gnomadrs17881233
Varsomers17881233
LitVarrs17881233
Maprs17881233
PheGenIrs17881233
Biobankrs17881233
1000 genomesrs17881233
hgdprs17881233
ensemblrs17881233
geneviewrs17881233
scholarrs17881233
googlers17881233
pharmgkbrs17881233
gwascentralrs17881233
openSNPrs17881233
23andMers17881233
SNPshotrs17881233
SNPdbers17881233
MSV3drs17881233
GWAS Ctlgrs17881233
GMAF0.03306
Max Magnitude0
ClinVar
Risk rs17881233(T;T)
Alt rs17881233(T;T)
Reference Rs17881233(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323745C>A
CLNSRC
CLNACC