Have questions? Visit https://www.reddit.com/r/SNPedia

rs41542121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41542121(C;C)
Make rs41542121(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356885
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41542121
ebirs41542121
HLIrs41542121
Exacrs41542121
Varsomers41542121
Maprs41542121
PheGenIrs41542121
hapmaprs41542121
1000 genomesrs41542121
hgdprs41542121
ensemblrs41542121
gopubmedrs41542121
geneviewrs41542121
scholarrs41542121
googlers41542121
pharmgkbrs41542121
gwascentralrs41542121
openSNPrs41542121
23andMers41542121
23andMe allrs41542121
SNP Nexus

SNPshotrs41542121
SNPdbers41542121
MSV3drs41542121
GWAS Ctlgrs41542121
Max Magnitude0
ClinVar
Risk rs41542121(C;C)
Alt rs41542121(C;C)
Reference rs41542121(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324662A>G
CLNSRC
CLNACC