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rs41551018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551018(G;T)
Make rs41551018(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356274
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551018
ebirs41551018
HLIrs41551018
Exacrs41551018
Varsomers41551018
Maprs41551018
PheGenIrs41551018
hapmaprs41551018
1000 genomesrs41551018
hgdprs41551018
ensemblrs41551018
gopubmedrs41551018
geneviewrs41551018
scholarrs41551018
googlers41551018
pharmgkbrs41551018
gwascentralrs41551018
openSNPrs41551018
23andMers41551018
23andMe allrs41551018
SNP Nexus

SNPshotrs41551018
SNPdbers41551018
MSV3drs41551018
GWAS Ctlgrs41551018
GMAF0.07484
Max Magnitude0
ClinVar
Risk rs41551018(T;T)
Alt rs41551018(T;T)
Reference rs41551018(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324051C>A
CLNSRC
CLNACC