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rs2523600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2523600(C;C)
Make rs2523600(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356227
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs2523600
dbSNP (classic)rs2523600
ClinGenrs2523600
ebirs2523600
HLIrs2523600
Exacrs2523600
Gnomadrs2523600
Varsomers2523600
LitVarrs2523600
Maprs2523600
PheGenIrs2523600
Biobankrs2523600
1000 genomesrs2523600
hgdprs2523600
ensemblrs2523600
geneviewrs2523600
scholarrs2523600
googlers2523600
pharmgkbrs2523600
gwascentralrs2523600
openSNPrs2523600
23andMers2523600
SNPshotrs2523600
SNPdbers2523600
MSV3drs2523600
GWAS Ctlgrs2523600
GMAF0.4766
Max Magnitude0
ClinVar
Risk rs2523600(A;A) rs2523600(C;C)
Alt rs2523600(A;A) rs2523600(C;C)
Reference Rs2523600(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324004C>G; NC_000006.11:g.31324004C>T
CLNSRC
CLNACC