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rs41543314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41543314(C;C)
Make rs41543314(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354913
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41543314
ebirs41543314
HLIrs41543314
Exacrs41543314
Varsomers41543314
Maprs41543314
PheGenIrs41543314
hapmaprs41543314
1000 genomesrs41543314
hgdprs41543314
ensemblrs41543314
gopubmedrs41543314
geneviewrs41543314
scholarrs41543314
googlers41543314
pharmgkbrs41543314
gwascentralrs41543314
openSNPrs41543314
23andMers41543314
23andMe allrs41543314
SNP Nexus

SNPshotrs41543314
SNPdbers41543314
MSV3drs41543314
GWAS Ctlgrs41543314
GMAF0.02755
Max Magnitude0
ClinVar
Risk rs41543314(C;C)
Alt rs41543314(C;C)
Reference rs41543314(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322690A>G
CLNSRC
CLNACC