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rs41542717

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41542717(C;T)
Make rs41542717(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355153
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41542717
ebirs41542717
HLIrs41542717
Exacrs41542717
Varsomers41542717
Maprs41542717
PheGenIrs41542717
hapmaprs41542717
1000 genomesrs41542717
hgdprs41542717
ensemblrs41542717
gopubmedrs41542717
geneviewrs41542717
scholarrs41542717
googlers41542717
pharmgkbrs41542717
gwascentralrs41542717
openSNPrs41542717
23andMers41542717
23andMe allrs41542717
SNP Nexus

SNPshotrs41542717
SNPdbers41542717
MSV3drs41542717
GWAS Ctlgrs41542717
Max Magnitude0
ClinVar
Risk rs41542717(T;T)
Alt rs41542717(T;T)
Reference rs41542717(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322930G>A
CLNSRC
CLNACC