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rs41546213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546213(C;G)
Make rs41546213(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356860
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546213
ebirs41546213
HLIrs41546213
Exacrs41546213
Varsomers41546213
Maprs41546213
PheGenIrs41546213
hapmaprs41546213
1000 genomesrs41546213
hgdprs41546213
ensemblrs41546213
gopubmedrs41546213
geneviewrs41546213
scholarrs41546213
googlers41546213
pharmgkbrs41546213
gwascentralrs41546213
openSNPrs41546213
23andMers41546213
23andMe allrs41546213
SNP Nexus

SNPshotrs41546213
SNPdbers41546213
MSV3drs41546213
GWAS Ctlgrs41546213
Max Magnitude0
ClinVar
Risk rs41546213(G,T;G,T)
Alt rs41546213(G,T;G,T)
Reference rs41546213(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324637G>A; NC_000006.11:g.31324637G>C
CLNSRC
CLNACC