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rs1050642

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050642(A;A)
Make rs1050642(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356351
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050642
ebirs1050642
HLIrs1050642
Exacrs1050642
Varsomers1050642
Maprs1050642
PheGenIrs1050642
hapmaprs1050642
1000 genomesrs1050642
hgdprs1050642
ensemblrs1050642
gopubmedrs1050642
geneviewrs1050642
scholarrs1050642
googlers1050642
pharmgkbrs1050642
gwascentralrs1050642
openSNPrs1050642
23andMers1050642
23andMe allrs1050642
SNP Nexus

SNPshotrs1050642
SNPdbers1050642
MSV3drs1050642
GWAS Ctlgrs1050642
GMAF0.07254
Max Magnitude0
ClinVar
Risk rs1050642(A;A)
Alt rs1050642(A;A)
Reference rs1050642(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324128C>T
CLNSRC
CLNACC