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rs72558118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558118(C;C)
Make rs72558118(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356239
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs72558118
dbSNP (classic)rs72558118
ClinGenrs72558118
ebirs72558118
HLIrs72558118
Exacrs72558118
Gnomadrs72558118
Varsomers72558118
LitVarrs72558118
Maprs72558118
PheGenIrs72558118
Biobankrs72558118
1000 genomesrs72558118
hgdprs72558118
ensemblrs72558118
geneviewrs72558118
scholarrs72558118
googlers72558118
pharmgkbrs72558118
gwascentralrs72558118
openSNPrs72558118
23andMers72558118
SNPshotrs72558118
SNPdbers72558118
MSV3drs72558118
GWAS Ctlgrs72558118
Max Magnitude0
ClinVar
Risk rs72558118(C;C)
Alt rs72558118(C;C)
Reference Rs72558118(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324016A>G
CLNSRC
CLNACC