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rs41556218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41556218(C;C)
Make rs41556218(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356121
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556218
ebirs41556218
HLIrs41556218
Exacrs41556218
Varsomers41556218
Maprs41556218
PheGenIrs41556218
hapmaprs41556218
1000 genomesrs41556218
hgdprs41556218
ensemblrs41556218
gopubmedrs41556218
geneviewrs41556218
scholarrs41556218
googlers41556218
pharmgkbrs41556218
gwascentralrs41556218
openSNPrs41556218
23andMers41556218
23andMe allrs41556218
SNP Nexus

SNPshotrs41556218
SNPdbers41556218
MSV3drs41556218
GWAS Ctlgrs41556218
Max Magnitude0
ClinVar
Risk rs41556218(C;C)
Alt rs41556218(C;C)
Reference rs41556218(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323898C>G
CLNSRC
CLNACC