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rs41552313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41552313(A;G)
Make rs41552313(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356102
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552313
ebirs41552313
HLIrs41552313
Exacrs41552313
Varsomers41552313
Maprs41552313
PheGenIrs41552313
hapmaprs41552313
1000 genomesrs41552313
hgdprs41552313
ensemblrs41552313
gopubmedrs41552313
geneviewrs41552313
scholarrs41552313
googlers41552313
pharmgkbrs41552313
gwascentralrs41552313
openSNPrs41552313
23andMers41552313
23andMe allrs41552313
SNP Nexus

SNPshotrs41552313
SNPdbers41552313
MSV3drs41552313
GWAS Ctlgrs41552313
Max Magnitude0
ClinVar
Risk rs41552313(G;G)
Alt rs41552313(G;G)
Reference rs41552313(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323879T>C
CLNSRC
CLNACC