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rs41549118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41549118(A;A)
Make rs41549118(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356569
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41549118
ebirs41549118
HLIrs41549118
Exacrs41549118
Varsomers41549118
Maprs41549118
PheGenIrs41549118
hapmaprs41549118
1000 genomesrs41549118
hgdprs41549118
ensemblrs41549118
gopubmedrs41549118
geneviewrs41549118
scholarrs41549118
googlers41549118
pharmgkbrs41549118
gwascentralrs41549118
openSNPrs41549118
23andMers41549118
23andMe allrs41549118
SNP Nexus

SNPshotrs41549118
SNPdbers41549118
MSV3drs41549118
GWAS Ctlgrs41549118
Max Magnitude0
ClinVar
Risk rs41549118(A;A)
Alt rs41549118(A;A)
Reference rs41549118(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324346G>T
CLNSRC
CLNACC