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rs41545518

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545518(C;T)
Make rs41545518(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355830
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545518
ebirs41545518
HLIrs41545518
Exacrs41545518
Varsomers41545518
Maprs41545518
PheGenIrs41545518
hapmaprs41545518
1000 genomesrs41545518
hgdprs41545518
ensemblrs41545518
gopubmedrs41545518
geneviewrs41545518
scholarrs41545518
googlers41545518
pharmgkbrs41545518
gwascentralrs41545518
openSNPrs41545518
23andMers41545518
23andMe allrs41545518
SNP Nexus

SNPshotrs41545518
SNPdbers41545518
MSV3drs41545518
GWAS Ctlgrs41545518
Max Magnitude0
ClinVar
Risk rs41545518(T;T)
Alt rs41545518(T;T)
Reference rs41545518(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323607G>A
CLNSRC
CLNACC