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rs114038515

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs114038515(C;T)
Make rs114038515(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357164
GeneHLA-B
is asnp
is mentioned by
dbSNPrs114038515
ebirs114038515
HLIrs114038515
Exacrs114038515
Varsomers114038515
Maprs114038515
PheGenIrs114038515
hapmaprs114038515
1000 genomesrs114038515
hgdprs114038515
ensemblrs114038515
gopubmedrs114038515
geneviewrs114038515
scholarrs114038515
googlers114038515
pharmgkbrs114038515
gwascentralrs114038515
openSNPrs114038515
23andMers114038515
23andMe allrs114038515
SNP Nexus

SNPshotrs114038515
SNPdbers114038515
MSV3drs114038515
GWAS Ctlgrs114038515
GMAF0.03076
Max Magnitude0
ClinVar
Risk rs114038515(T;T)
Alt rs114038515(T;T)
Reference rs114038515(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324941C>T
CLNSRC
CLNACC