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rs114811870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs114811870(C;T)
Make rs114811870(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357161
GeneHLA-B
is asnp
is mentioned by
dbSNPrs114811870
ebirs114811870
HLIrs114811870
Exacrs114811870
Varsomers114811870
Maprs114811870
PheGenIrs114811870
hapmaprs114811870
1000 genomesrs114811870
hgdprs114811870
ensemblrs114811870
gopubmedrs114811870
geneviewrs114811870
scholarrs114811870
googlers114811870
pharmgkbrs114811870
gwascentralrs114811870
openSNPrs114811870
23andMers114811870
23andMe allrs114811870
SNP Nexus

SNPshotrs114811870
SNPdbers114811870
MSV3drs114811870
GWAS Ctlgrs114811870
GMAF0.02571
Max Magnitude0
ClinVar
Risk rs114811870(T;T)
Alt rs114811870(T;T)
Reference rs114811870(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324938C>T
CLNSRC
CLNACC