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rs76032827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs76032827(-;-)
Make rs76032827(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356915
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs76032827
dbSNP (classic)rs76032827
ClinGenrs76032827
ebirs76032827
HLIrs76032827
Exacrs76032827
Gnomadrs76032827
Varsomers76032827
LitVarrs76032827
Maprs76032827
PheGenIrs76032827
Biobankrs76032827
1000 genomesrs76032827
hgdprs76032827
ensemblrs76032827
geneviewrs76032827
scholarrs76032827
googlers76032827
pharmgkbrs76032827
gwascentralrs76032827
openSNPrs76032827
23andMers76032827
SNPshotrs76032827
SNPdbers76032827
MSV3drs76032827
GWAS Ctlgrs76032827
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs76032827(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324692delG
CLNSRC
CLNACC