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rs41546617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41546617(G;G)
Make rs41546617(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356938
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546617
ebirs41546617
HLIrs41546617
Exacrs41546617
Varsomers41546617
Maprs41546617
PheGenIrs41546617
hapmaprs41546617
1000 genomesrs41546617
hgdprs41546617
ensemblrs41546617
gopubmedrs41546617
geneviewrs41546617
scholarrs41546617
googlers41546617
pharmgkbrs41546617
gwascentralrs41546617
openSNPrs41546617
23andMers41546617
23andMe allrs41546617
SNP Nexus

SNPshotrs41546617
SNPdbers41546617
MSV3drs41546617
GWAS Ctlgrs41546617
Max Magnitude0
ClinVar
Risk rs41546617(C,G;C,G)
Alt rs41546617(C,G;C,G)
Reference rs41546617(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324715A>C; NC_000006.11:g.31324715A>G
CLNSRC
CLNACC