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rs1050388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050388(A;A)
Make rs1050388(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356729
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050388
ebirs1050388
HLIrs1050388
Exacrs1050388
Varsomers1050388
Maprs1050388
PheGenIrs1050388
hapmaprs1050388
1000 genomesrs1050388
hgdprs1050388
ensemblrs1050388
gopubmedrs1050388
geneviewrs1050388
scholarrs1050388
googlers1050388
pharmgkbrs1050388
gwascentralrs1050388
openSNPrs1050388
23andMers1050388
23andMe allrs1050388
SNP Nexus

SNPshotrs1050388
SNPdbers1050388
MSV3drs1050388
GWAS Ctlgrs1050388
GMAF0.2181
Max Magnitude0
ClinVar
Risk rs1050388(A,C;A,C)
Alt rs1050388(A,C;A,C)
Reference rs1050388(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324506C>G; NC_000006.11:g.31324506C>T
CLNSRC
CLNACC