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rs41540116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41540116(C;C)
Make rs41540116(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357103
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41540116
ebirs41540116
HLIrs41540116
Exacrs41540116
Varsomers41540116
Maprs41540116
PheGenIrs41540116
hapmaprs41540116
1000 genomesrs41540116
hgdprs41540116
ensemblrs41540116
gopubmedrs41540116
geneviewrs41540116
scholarrs41540116
googlers41540116
pharmgkbrs41540116
gwascentralrs41540116
openSNPrs41540116
23andMers41540116
23andMe allrs41540116
SNP Nexus

SNPshotrs41540116
SNPdbers41540116
MSV3drs41540116
GWAS Ctlgrs41540116
Max Magnitude0
ClinVar
Risk rs41540116(C;C)
Alt rs41540116(C;C)
Reference rs41540116(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324880A>G
CLNSRC
CLNACC