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rs41554418

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41554418(A;A)
Make rs41554418(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356173
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41554418
ebirs41554418
HLIrs41554418
Exacrs41554418
Varsomers41554418
Maprs41554418
PheGenIrs41554418
hapmaprs41554418
1000 genomesrs41554418
hgdprs41554418
ensemblrs41554418
gopubmedrs41554418
geneviewrs41554418
scholarrs41554418
googlers41554418
pharmgkbrs41554418
gwascentralrs41554418
openSNPrs41554418
23andMers41554418
23andMe allrs41554418
SNP Nexus

SNPshotrs41554418
SNPdbers41554418
MSV3drs41554418
GWAS Ctlgrs41554418
Max Magnitude0
ClinVar
Risk rs41554418(A,G,T;A,G,T)
Alt rs41554418(A,G,T;A,G,T)
Reference rs41554418(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323950G>A; NC_000006.11:g.31323950G>C; NC_000006.11:g.31323950G>T
CLNSRC
CLNACC