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rs41554617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41554617(C;T)
Make rs41554617(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355730
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41554617
ebirs41554617
HLIrs41554617
Exacrs41554617
Varsomers41554617
Maprs41554617
PheGenIrs41554617
hapmaprs41554617
1000 genomesrs41554617
hgdprs41554617
ensemblrs41554617
gopubmedrs41554617
geneviewrs41554617
scholarrs41554617
googlers41554617
pharmgkbrs41554617
gwascentralrs41554617
openSNPrs41554617
23andMers41554617
23andMe allrs41554617
SNP Nexus

SNPshotrs41554617
SNPdbers41554617
MSV3drs41554617
GWAS Ctlgrs41554617
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs41554617(T;T)
Alt rs41554617(T;T)
Reference rs41554617(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323507G>A
CLNSRC
CLNACC