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rs1050686

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050686(C;T)
Make rs1050686(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271132
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050686
ebirs1050686
HLIrs1050686
Exacrs1050686
Varsomers1050686
Maprs1050686
PheGenIrs1050686
hapmaprs1050686
1000 genomesrs1050686
hgdprs1050686
ensemblrs1050686
gopubmedrs1050686
geneviewrs1050686
scholarrs1050686
googlers1050686
pharmgkbrs1050686
gwascentralrs1050686
openSNPrs1050686
23andMers1050686
23andMe allrs1050686
SNP Nexus

SNPshotrs1050686
SNPdbers1050686
MSV3drs1050686
GWAS Ctlgrs1050686
Max Magnitude0
ClinVar
Risk rs1050686(A,T;A,T)
Alt rs1050686(A,T;A,T)
Reference rs1050686(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238909G>A; NC_000006.11:g.31238909G>T
CLNSRC
CLNACC