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rs709052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs709052(C;C)
Make rs709052(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355456
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs709052
dbSNP (classic)rs709052
ClinGenrs709052
ebirs709052
HLIrs709052
Exacrs709052
Gnomadrs709052
Varsomers709052
LitVarrs709052
Maprs709052
PheGenIrs709052
Biobankrs709052
1000 genomesrs709052
hgdprs709052
ensemblrs709052
geneviewrs709052
scholarrs709052
googlers709052
pharmgkbrs709052
gwascentralrs709052
openSNPrs709052
23andMers709052
SNPshotrs709052
SNPdbers709052
MSV3drs709052
GWAS Ctlgrs709052
GMAF0.4224
Max Magnitude0
ClinVar
Risk rs709052(C;C) rs709052(G;G)
Alt rs709052(C;C) rs709052(G;G)
Reference Rs709052(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323233A>C; NC_000006.11:g.31323233A>G
CLNSRC
CLNACC