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rs1050105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050105(C;T)
Make rs1050105(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269992
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050105
ebirs1050105
HLIrs1050105
Exacrs1050105
Varsomers1050105
Maprs1050105
PheGenIrs1050105
hapmaprs1050105
1000 genomesrs1050105
hgdprs1050105
ensemblrs1050105
gopubmedrs1050105
geneviewrs1050105
scholarrs1050105
googlers1050105
pharmgkbrs1050105
gwascentralrs1050105
openSNPrs1050105
23andMers1050105
23andMe allrs1050105
SNP Nexus

SNPshotrs1050105
SNPdbers1050105
MSV3drs1050105
GWAS Ctlgrs1050105
Max Magnitude0
ClinVar
Risk rs1050105(T;T)
Alt rs1050105(T;T)
Reference rs1050105(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237769G>A
CLNSRC
CLNACC