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rs41543121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41543121(A;A)
Make rs41543121(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356760
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41543121
ebirs41543121
HLIrs41543121
Exacrs41543121
Varsomers41543121
Maprs41543121
PheGenIrs41543121
hapmaprs41543121
1000 genomesrs41543121
hgdprs41543121
ensemblrs41543121
gopubmedrs41543121
geneviewrs41543121
scholarrs41543121
googlers41543121
pharmgkbrs41543121
gwascentralrs41543121
openSNPrs41543121
23andMers41543121
23andMe allrs41543121
SNP Nexus

SNPshotrs41543121
SNPdbers41543121
MSV3drs41543121
GWAS Ctlgrs41543121
Max Magnitude0
ClinVar
Risk rs41543121(A,C,G;A,C,G)
Alt rs41543121(A,C,G;A,C,G)
Reference rs41543121(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324537A>C; NC_000006.11:g.31324537A>G; NC_000006.11:g.31324537A>T
CLNSRC
CLNACC