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rs41549217

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41549217(A;A)
Make rs41549217(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356108
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41549217
ebirs41549217
HLIrs41549217
Exacrs41549217
Varsomers41549217
Maprs41549217
PheGenIrs41549217
hapmaprs41549217
1000 genomesrs41549217
hgdprs41549217
ensemblrs41549217
gopubmedrs41549217
geneviewrs41549217
scholarrs41549217
googlers41549217
pharmgkbrs41549217
gwascentralrs41549217
openSNPrs41549217
23andMers41549217
23andMe allrs41549217
SNP Nexus

SNPshotrs41549217
SNPdbers41549217
MSV3drs41549217
GWAS Ctlgrs41549217
GMAF0.04913
Max Magnitude0
ClinVar
Risk rs41549217(A;A)
Alt rs41549217(A;A)
Reference rs41549217(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323885G>T
CLNSRC
CLNACC