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rs1050368

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050368(A;A)
Make rs1050368(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356301
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050368
ebirs1050368
HLIrs1050368
Exacrs1050368
Varsomers1050368
Maprs1050368
PheGenIrs1050368
hapmaprs1050368
1000 genomesrs1050368
hgdprs1050368
ensemblrs1050368
gopubmedrs1050368
geneviewrs1050368
scholarrs1050368
googlers1050368
pharmgkbrs1050368
gwascentralrs1050368
openSNPrs1050368
23andMers1050368
23andMe allrs1050368
SNP Nexus

SNPshotrs1050368
SNPdbers1050368
MSV3drs1050368
GWAS Ctlgrs1050368
GMAF0.03994
Max Magnitude0
ClinVar
Risk rs1050368(A,G;A,G)
Alt rs1050368(A,G;A,G)
Reference rs1050368(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324078G>T
CLNSRC
CLNACC