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rs41552516

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41552516(C;T)
Make rs41552516(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356840
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552516
ebirs41552516
HLIrs41552516
Exacrs41552516
Varsomers41552516
Maprs41552516
PheGenIrs41552516
hapmaprs41552516
1000 genomesrs41552516
hgdprs41552516
ensemblrs41552516
gopubmedrs41552516
geneviewrs41552516
scholarrs41552516
googlers41552516
pharmgkbrs41552516
gwascentralrs41552516
openSNPrs41552516
23andMers41552516
23andMe allrs41552516
SNP Nexus

SNPshotrs41552516
SNPdbers41552516
MSV3drs41552516
GWAS Ctlgrs41552516
Max Magnitude0
ClinVar
Risk rs41552516(G,T;G,T)
Alt rs41552516(G,T;G,T)
Reference rs41552516(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324617G>A; NC_000006.11:g.31324617G>C
CLNSRC
CLNACC