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rs41558422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41558422(C;C)
Make rs41558422(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356883
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558422
ebirs41558422
HLIrs41558422
Exacrs41558422
Varsomers41558422
Maprs41558422
PheGenIrs41558422
hapmaprs41558422
1000 genomesrs41558422
hgdprs41558422
ensemblrs41558422
gopubmedrs41558422
geneviewrs41558422
scholarrs41558422
googlers41558422
pharmgkbrs41558422
gwascentralrs41558422
openSNPrs41558422
23andMers41558422
23andMe allrs41558422
SNP Nexus

SNPshotrs41558422
SNPdbers41558422
MSV3drs41558422
GWAS Ctlgrs41558422
Max Magnitude0
ClinVar
Risk rs41558422(C;C)
Alt rs41558422(C;C)
Reference rs41558422(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324660C>G
CLNSRC
CLNACC