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rs1050106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050106(C;T)
Make rs1050106(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269994
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050106
ClinGenrs1050106
ebirs1050106
HLIrs1050106
Exacrs1050106
Varsomers1050106
Maprs1050106
PheGenIrs1050106
hapmaprs1050106
1000 genomesrs1050106
hgdprs1050106
ensemblrs1050106
gopubmedrs1050106
geneviewrs1050106
scholarrs1050106
googlers1050106
pharmgkbrs1050106
gwascentralrs1050106
openSNPrs1050106
23andMers1050106
23andMe allrs1050106
SNP Nexus

SNPshotrs1050106
SNPdbers1050106
MSV3drs1050106
GWAS Ctlgrs1050106
GMAF0.3958
Max Magnitude0
ClinVar
Risk rs1050106(T;T)
Alt rs1050106(T;T)
Reference Rs1050106(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237771G>A
CLNSRC
CLNACC