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rs41562715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41562715(A;C)
Make rs41562715(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355147
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562715
ebirs41562715
HLIrs41562715
Exacrs41562715
Varsomers41562715
Maprs41562715
PheGenIrs41562715
hapmaprs41562715
1000 genomesrs41562715
hgdprs41562715
ensemblrs41562715
gopubmedrs41562715
geneviewrs41562715
scholarrs41562715
googlers41562715
pharmgkbrs41562715
gwascentralrs41562715
openSNPrs41562715
23andMers41562715
23andMe allrs41562715
SNP Nexus

SNPshotrs41562715
SNPdbers41562715
MSV3drs41562715
GWAS Ctlgrs41562715
Max Magnitude0
ClinVar
Risk rs41562715(C;C)
Alt rs41562715(C;C)
Reference rs41562715(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322924T>G
CLNSRC
CLNACC