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rs41562514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562514(C;T)
Make rs41562514(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356514
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562514
ebirs41562514
HLIrs41562514
Exacrs41562514
Varsomers41562514
Maprs41562514
PheGenIrs41562514
hapmaprs41562514
1000 genomesrs41562514
hgdprs41562514
ensemblrs41562514
gopubmedrs41562514
geneviewrs41562514
scholarrs41562514
googlers41562514
pharmgkbrs41562514
gwascentralrs41562514
openSNPrs41562514
23andMers41562514
23andMe allrs41562514
SNP Nexus

SNPshotrs41562514
SNPdbers41562514
MSV3drs41562514
GWAS Ctlgrs41562514
Max Magnitude0
ClinVar
Risk rs41562514(T;T)
Alt rs41562514(T;T)
Reference rs41562514(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324291G>A
CLNSRC
CLNACC