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rs41546518

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41546518(A;T)
Make rs41546518(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356756
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546518
ebirs41546518
HLIrs41546518
Exacrs41546518
Varsomers41546518
Maprs41546518
PheGenIrs41546518
hapmaprs41546518
1000 genomesrs41546518
hgdprs41546518
ensemblrs41546518
gopubmedrs41546518
geneviewrs41546518
scholarrs41546518
googlers41546518
pharmgkbrs41546518
gwascentralrs41546518
openSNPrs41546518
23andMers41546518
23andMe allrs41546518
SNP Nexus

SNPshotrs41546518
SNPdbers41546518
MSV3drs41546518
GWAS Ctlgrs41546518
Max Magnitude0
ClinVar
Risk rs41546518(T;T)
Alt rs41546518(T;T)
Reference rs41546518(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324533T>A
CLNSRC
CLNACC