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rs41555513

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555513(C;T)
Make rs41555513(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355703
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41555513
ebirs41555513
HLIrs41555513
Exacrs41555513
Varsomers41555513
Maprs41555513
PheGenIrs41555513
hapmaprs41555513
1000 genomesrs41555513
hgdprs41555513
ensemblrs41555513
gopubmedrs41555513
geneviewrs41555513
scholarrs41555513
googlers41555513
pharmgkbrs41555513
gwascentralrs41555513
openSNPrs41555513
23andMers41555513
23andMe allrs41555513
SNP Nexus

SNPshotrs41555513
SNPdbers41555513
MSV3drs41555513
GWAS Ctlgrs41555513
GMAF0.02479
Max Magnitude0
ClinVar
Risk rs41555513(T;T)
Alt rs41555513(T;T)
Reference rs41555513(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323480G>A
CLNSRC
CLNACC