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rs41548118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41548118(A;A)
Make rs41548118(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356083
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548118
ebirs41548118
HLIrs41548118
Exacrs41548118
Varsomers41548118
Maprs41548118
PheGenIrs41548118
hapmaprs41548118
1000 genomesrs41548118
hgdprs41548118
ensemblrs41548118
gopubmedrs41548118
geneviewrs41548118
scholarrs41548118
googlers41548118
pharmgkbrs41548118
gwascentralrs41548118
openSNPrs41548118
23andMers41548118
23andMe allrs41548118
SNP Nexus

SNPshotrs41548118
SNPdbers41548118
MSV3drs41548118
GWAS Ctlgrs41548118
Max Magnitude0
ClinVar
Risk rs41548118(A;A)
Alt rs41548118(A;A)
Reference rs41548118(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323860G>T
CLNSRC
CLNACC