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rs41553912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553912(A;A)
Make rs41553912(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356360
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553912
ebirs41553912
HLIrs41553912
Exacrs41553912
Varsomers41553912
Maprs41553912
PheGenIrs41553912
hapmaprs41553912
1000 genomesrs41553912
hgdprs41553912
ensemblrs41553912
gopubmedrs41553912
geneviewrs41553912
scholarrs41553912
googlers41553912
pharmgkbrs41553912
gwascentralrs41553912
openSNPrs41553912
23andMers41553912
23andMe allrs41553912
SNP Nexus

SNPshotrs41553912
SNPdbers41553912
MSV3drs41553912
GWAS Ctlgrs41553912
Max Magnitude0
ClinVar
Risk rs41553912(A;A)
Alt rs41553912(A;A)
Reference rs41553912(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324137G>T
CLNSRC
CLNACC