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rs41557218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557218(A;A)
Make rs41557218(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356127
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557218
ebirs41557218
HLIrs41557218
Exacrs41557218
Varsomers41557218
Maprs41557218
PheGenIrs41557218
hapmaprs41557218
1000 genomesrs41557218
hgdprs41557218
ensemblrs41557218
gopubmedrs41557218
geneviewrs41557218
scholarrs41557218
googlers41557218
pharmgkbrs41557218
gwascentralrs41557218
openSNPrs41557218
23andMers41557218
23andMe allrs41557218
SNP Nexus

SNPshotrs41557218
SNPdbers41557218
MSV3drs41557218
GWAS Ctlgrs41557218
Max Magnitude0
ClinVar
Risk rs41557218(A;A)
Alt rs41557218(A;A)
Reference rs41557218(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323904C>T
CLNSRC
CLNACC