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rs72558120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558120(A;A)
Make rs72558120(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355470
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs72558120
dbSNP (classic)rs72558120
ClinGenrs72558120
ebirs72558120
HLIrs72558120
Exacrs72558120
Gnomadrs72558120
Varsomers72558120
LitVarrs72558120
Maprs72558120
PheGenIrs72558120
Biobankrs72558120
1000 genomesrs72558120
hgdprs72558120
ensemblrs72558120
geneviewrs72558120
scholarrs72558120
googlers72558120
pharmgkbrs72558120
gwascentralrs72558120
openSNPrs72558120
23andMers72558120
SNPshotrs72558120
SNPdbers72558120
MSV3drs72558120
GWAS Ctlgrs72558120
Max Magnitude0
ClinVar
Risk rs72558120(A;A)
Alt rs72558120(A;A)
Reference Rs72558120(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323247G>T
CLNSRC
CLNACC