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rs41553417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41553417(A;A)
Make rs41553417(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356262
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553417
ebirs41553417
HLIrs41553417
Exacrs41553417
Varsomers41553417
Maprs41553417
PheGenIrs41553417
hapmaprs41553417
1000 genomesrs41553417
hgdprs41553417
ensemblrs41553417
gopubmedrs41553417
geneviewrs41553417
scholarrs41553417
googlers41553417
pharmgkbrs41553417
gwascentralrs41553417
openSNPrs41553417
23andMers41553417
23andMe allrs41553417
SNP Nexus

SNPshotrs41553417
SNPdbers41553417
MSV3drs41553417
GWAS Ctlgrs41553417
Max Magnitude0
ClinVar
Risk rs41553417(A,C,T;A,C,T)
Alt rs41553417(A,C,T;A,C,T)
Reference rs41553417(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324039C>A; NC_000006.11:g.31324039C>G; NC_000006.11:g.31324039C>T
CLNSRC
CLNACC