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rs1050486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050486(A;A)
Make rs1050486(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356925
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050486
ebirs1050486
HLIrs1050486
Exacrs1050486
Varsomers1050486
Maprs1050486
PheGenIrs1050486
hapmaprs1050486
1000 genomesrs1050486
hgdprs1050486
ensemblrs1050486
gopubmedrs1050486
geneviewrs1050486
scholarrs1050486
googlers1050486
pharmgkbrs1050486
gwascentralrs1050486
openSNPrs1050486
23andMers1050486
23andMe allrs1050486
SNP Nexus

SNPshotrs1050486
SNPdbers1050486
MSV3drs1050486
GWAS Ctlgrs1050486
GMAF0.3935
Max Magnitude0
ClinVar
Risk rs1050486(A,C;A,C)
Alt rs1050486(A,C;A,C)
Reference rs1050486(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324702C>G; NC_000006.11:g.31324702C>T
CLNSRC
CLNACC