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rs41552819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552819(G;T)
Make rs41552819(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356378
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552819
ebirs41552819
HLIrs41552819
Exacrs41552819
Varsomers41552819
Maprs41552819
PheGenIrs41552819
hapmaprs41552819
1000 genomesrs41552819
hgdprs41552819
ensemblrs41552819
gopubmedrs41552819
geneviewrs41552819
scholarrs41552819
googlers41552819
pharmgkbrs41552819
gwascentralrs41552819
openSNPrs41552819
23andMers41552819
23andMe allrs41552819
SNP Nexus

SNPshotrs41552819
SNPdbers41552819
MSV3drs41552819
GWAS Ctlgrs41552819
Max Magnitude0
ClinVar
Risk rs41552819(T;T)
Alt rs41552819(T;T)
Reference rs41552819(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324155C>A
CLNSRC
CLNACC