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rs41552116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552116(G;T)
Make rs41552116(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357021
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552116
ebirs41552116
HLIrs41552116
Exacrs41552116
Varsomers41552116
Maprs41552116
PheGenIrs41552116
hapmaprs41552116
1000 genomesrs41552116
hgdprs41552116
ensemblrs41552116
gopubmedrs41552116
geneviewrs41552116
scholarrs41552116
googlers41552116
pharmgkbrs41552116
gwascentralrs41552116
openSNPrs41552116
23andMers41552116
23andMe allrs41552116
SNP Nexus

SNPshotrs41552116
SNPdbers41552116
MSV3drs41552116
GWAS Ctlgrs41552116
Max Magnitude0
ClinVar
Risk rs41552116(T;T)
Alt rs41552116(T;T)
Reference rs41552116(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324798C>A
CLNSRC
CLNACC