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rs41552913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552913(G;T)
Make rs41552913(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356466
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552913
ebirs41552913
HLIrs41552913
Exacrs41552913
Varsomers41552913
Maprs41552913
PheGenIrs41552913
hapmaprs41552913
1000 genomesrs41552913
hgdprs41552913
ensemblrs41552913
gopubmedrs41552913
geneviewrs41552913
scholarrs41552913
googlers41552913
pharmgkbrs41552913
gwascentralrs41552913
openSNPrs41552913
23andMers41552913
23andMe allrs41552913
SNP Nexus

SNPshotrs41552913
SNPdbers41552913
MSV3drs41552913
GWAS Ctlgrs41552913
Max Magnitude0
ClinVar
Risk rs41552913(T;T)
Alt rs41552913(T;T)
Reference rs41552913(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324243C>A
CLNSRC
CLNACC