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rs41541213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41541213(A;A)
Make rs41541213(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356736
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41541213
ebirs41541213
HLIrs41541213
Exacrs41541213
Varsomers41541213
Maprs41541213
PheGenIrs41541213
hapmaprs41541213
1000 genomesrs41541213
hgdprs41541213
ensemblrs41541213
gopubmedrs41541213
geneviewrs41541213
scholarrs41541213
googlers41541213
pharmgkbrs41541213
gwascentralrs41541213
openSNPrs41541213
23andMers41541213
23andMe allrs41541213
SNP Nexus

SNPshotrs41541213
SNPdbers41541213
MSV3drs41541213
GWAS Ctlgrs41541213
Max Magnitude0
ClinVar
Risk rs41541213(A,G,T;A,G,T)
Alt rs41541213(A,G,T;A,G,T)
Reference rs41541213(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324513G>A; NC_000006.11:g.31324513G>C; NC_000006.11:g.31324513G>T
CLNSRC
CLNACC