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rs41556417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41556417(A;G)
Make rs41556417(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356425
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556417
ebirs41556417
HLIrs41556417
Exacrs41556417
Varsomers41556417
Maprs41556417
PheGenIrs41556417
hapmaprs41556417
1000 genomesrs41556417
hgdprs41556417
ensemblrs41556417
gopubmedrs41556417
geneviewrs41556417
scholarrs41556417
googlers41556417
pharmgkbrs41556417
gwascentralrs41556417
openSNPrs41556417
23andMers41556417
23andMe allrs41556417
SNP Nexus

SNPshotrs41556417
SNPdbers41556417
MSV3drs41556417
GWAS Ctlgrs41556417
Max Magnitude0
ClinVar
Risk rs41556417(G,T;G,T)
Alt rs41556417(G,T;G,T)
Reference rs41556417(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324202T>A; NC_000006.11:g.31324202T>C
CLNSRC
CLNACC