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rs2523604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2523604(A;G)
Make rs2523604(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355989
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs2523604
dbSNP (classic)rs2523604
ClinGenrs2523604
ebirs2523604
HLIrs2523604
Exacrs2523604
Gnomadrs2523604
Varsomers2523604
LitVarrs2523604
Maprs2523604
PheGenIrs2523604
Biobankrs2523604
1000 genomesrs2523604
hgdprs2523604
ensemblrs2523604
geneviewrs2523604
scholarrs2523604
googlers2523604
pharmgkbrs2523604
gwascentralrs2523604
openSNPrs2523604
23andMers2523604
SNPshotrs2523604
SNPdbers2523604
MSV3drs2523604
GWAS Ctlgrs2523604
GMAF0.1745
Max Magnitude0
ClinVar
Risk rs2523604(G;G)
Alt rs2523604(G;G)
Reference Rs2523604(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323766T>C
CLNSRC
CLNACC