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rs41553017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553017(C;T)
Make rs41553017(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356613
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553017
ebirs41553017
HLIrs41553017
Exacrs41553017
Varsomers41553017
Maprs41553017
PheGenIrs41553017
hapmaprs41553017
1000 genomesrs41553017
hgdprs41553017
ensemblrs41553017
gopubmedrs41553017
geneviewrs41553017
scholarrs41553017
googlers41553017
pharmgkbrs41553017
gwascentralrs41553017
openSNPrs41553017
23andMers41553017
23andMe allrs41553017
SNP Nexus

SNPshotrs41553017
SNPdbers41553017
MSV3drs41553017
GWAS Ctlgrs41553017
Max Magnitude0
ClinVar
Risk rs41553017(T;T)
Alt rs41553017(T;T)
Reference rs41553017(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324390G>A
CLNSRC
CLNACC