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rs41556216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41556216(A;T)
Make rs41556216(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355108
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556216
ebirs41556216
HLIrs41556216
Exacrs41556216
Varsomers41556216
Maprs41556216
PheGenIrs41556216
hapmaprs41556216
1000 genomesrs41556216
hgdprs41556216
ensemblrs41556216
gopubmedrs41556216
geneviewrs41556216
scholarrs41556216
googlers41556216
pharmgkbrs41556216
gwascentralrs41556216
openSNPrs41556216
23andMers41556216
23andMe allrs41556216
SNP Nexus

SNPshotrs41556216
SNPdbers41556216
MSV3drs41556216
GWAS Ctlgrs41556216
GMAF0.007346
Max Magnitude0
ClinVar
Risk rs41556216(T;T)
Alt rs41556216(T;T)
Reference rs41556216(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322885T>A
CLNSRC
CLNACC