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rs41564218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41564218(C;T)
Make rs41564218(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355488
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41564218
ebirs41564218
HLIrs41564218
Exacrs41564218
Varsomers41564218
Maprs41564218
PheGenIrs41564218
hapmaprs41564218
1000 genomesrs41564218
hgdprs41564218
ensemblrs41564218
gopubmedrs41564218
geneviewrs41564218
scholarrs41564218
googlers41564218
pharmgkbrs41564218
gwascentralrs41564218
openSNPrs41564218
23andMers41564218
23andMe allrs41564218
SNP Nexus

SNPshotrs41564218
SNPdbers41564218
MSV3drs41564218
GWAS Ctlgrs41564218
Max Magnitude0
ClinVar
Risk rs41564218(T;T)
Alt rs41564218(T;T)
Reference rs41564218(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323265G>A
CLNSRC
CLNACC