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rs41553715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41553715(A;T)
Make rs41553715(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356732
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553715
ebirs41553715
HLIrs41553715
Exacrs41553715
Varsomers41553715
Maprs41553715
PheGenIrs41553715
hapmaprs41553715
1000 genomesrs41553715
hgdprs41553715
ensemblrs41553715
gopubmedrs41553715
geneviewrs41553715
scholarrs41553715
googlers41553715
pharmgkbrs41553715
gwascentralrs41553715
openSNPrs41553715
23andMers41553715
23andMe allrs41553715
SNP Nexus

SNPshotrs41553715
SNPdbers41553715
MSV3drs41553715
GWAS Ctlgrs41553715
GMAF0.0528
Max Magnitude0
ClinVar
Risk rs41553715(C,T;C,T)
Alt rs41553715(C,T;C,T)
Reference rs41553715(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324509T>A
CLNSRC
CLNACC