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rs41552314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41552314(C;C)
Make rs41552314(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356740
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552314
ebirs41552314
HLIrs41552314
Exacrs41552314
Varsomers41552314
Maprs41552314
PheGenIrs41552314
hapmaprs41552314
1000 genomesrs41552314
hgdprs41552314
ensemblrs41552314
gopubmedrs41552314
geneviewrs41552314
scholarrs41552314
googlers41552314
pharmgkbrs41552314
gwascentralrs41552314
openSNPrs41552314
23andMers41552314
23andMe allrs41552314
SNP Nexus

SNPshotrs41552314
SNPdbers41552314
MSV3drs41552314
GWAS Ctlgrs41552314
Max Magnitude0
ClinVar
Risk rs41552314(C;C)
Alt rs41552314(C;C)
Reference rs41552314(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324517A>G
CLNSRC
CLNACC