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rs41546814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546814(A;A)
Make rs41546814(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356867
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546814
ebirs41546814
HLIrs41546814
Exacrs41546814
Varsomers41546814
Maprs41546814
PheGenIrs41546814
hapmaprs41546814
1000 genomesrs41546814
hgdprs41546814
ensemblrs41546814
gopubmedrs41546814
geneviewrs41546814
scholarrs41546814
googlers41546814
pharmgkbrs41546814
gwascentralrs41546814
openSNPrs41546814
23andMers41546814
23andMe allrs41546814
SNP Nexus

SNPshotrs41546814
SNPdbers41546814
MSV3drs41546814
GWAS Ctlgrs41546814
Max Magnitude0
ClinVar
Risk rs41546814(A,T;A,T)
Alt rs41546814(A,T;A,T)
Reference rs41546814(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324644G>A; NC_000006.11:g.31324644G>T
CLNSRC
CLNACC