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rs2308559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2308559(A;A)
Make rs2308559(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356719
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs2308559
dbSNP (classic)rs2308559
ClinGenrs2308559
ebirs2308559
HLIrs2308559
Exacrs2308559
Gnomadrs2308559
Varsomers2308559
LitVarrs2308559
Maprs2308559
PheGenIrs2308559
Biobankrs2308559
1000 genomesrs2308559
hgdprs2308559
ensemblrs2308559
geneviewrs2308559
scholarrs2308559
googlers2308559
pharmgkbrs2308559
gwascentralrs2308559
openSNPrs2308559
23andMers2308559
SNPshotrs2308559
SNPdbers2308559
MSV3drs2308559
GWAS Ctlgrs2308559
Max Magnitude0
ClinVar
Risk rs2308559(A;A) rs2308559(G;G)
Alt rs2308559(A;A) rs2308559(G;G)
Reference Rs2308559(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324496G>C; NC_000006.11:g.31324496G>T
CLNSRC
CLNACC