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rs41552912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41552912(C;G)
Make rs41552912(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356642
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552912
ebirs41552912
HLIrs41552912
Exacrs41552912
Varsomers41552912
Maprs41552912
PheGenIrs41552912
hapmaprs41552912
1000 genomesrs41552912
hgdprs41552912
ensemblrs41552912
gopubmedrs41552912
geneviewrs41552912
scholarrs41552912
googlers41552912
pharmgkbrs41552912
gwascentralrs41552912
openSNPrs41552912
23andMers41552912
23andMe allrs41552912
SNP Nexus

SNPshotrs41552912
SNPdbers41552912
MSV3drs41552912
GWAS Ctlgrs41552912
Max Magnitude0
ClinVar
Risk rs41552912(G;G)
Alt rs41552912(G;G)
Reference rs41552912(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324419G>C
CLNSRC
CLNACC