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rs41551114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41551114(C;C)
Make rs41551114(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355160
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551114
ebirs41551114
HLIrs41551114
Exacrs41551114
Varsomers41551114
Maprs41551114
PheGenIrs41551114
hapmaprs41551114
1000 genomesrs41551114
hgdprs41551114
ensemblrs41551114
gopubmedrs41551114
geneviewrs41551114
scholarrs41551114
googlers41551114
pharmgkbrs41551114
gwascentralrs41551114
openSNPrs41551114
23andMers41551114
23andMe allrs41551114
SNP Nexus

SNPshotrs41551114
SNPdbers41551114
MSV3drs41551114
GWAS Ctlgrs41551114
Max Magnitude0
ClinVar
Risk rs41551114(C;C)
Alt rs41551114(C;C)
Reference rs41551114(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322937A>G
CLNSRC
CLNACC