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rs41551517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41551517(G;G)
Make rs41551517(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356215
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551517
ebirs41551517
HLIrs41551517
Exacrs41551517
Varsomers41551517
Maprs41551517
PheGenIrs41551517
hapmaprs41551517
1000 genomesrs41551517
hgdprs41551517
ensemblrs41551517
gopubmedrs41551517
geneviewrs41551517
scholarrs41551517
googlers41551517
pharmgkbrs41551517
gwascentralrs41551517
openSNPrs41551517
23andMers41551517
23andMe allrs41551517
SNP Nexus

SNPshotrs41551517
SNPdbers41551517
MSV3drs41551517
GWAS Ctlgrs41551517
Max Magnitude0
ClinVar
Risk rs41551517(C,G;C,G)
Alt rs41551517(C,G;C,G)
Reference rs41551517(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323992A>C; NC_000006.11:g.31323992A>G
CLNSRC
CLNACC