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rs1050118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050118(A;A)
Make rs1050118(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269999
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050118
ebirs1050118
HLIrs1050118
Exacrs1050118
Varsomers1050118
Maprs1050118
PheGenIrs1050118
hapmaprs1050118
1000 genomesrs1050118
hgdprs1050118
ensemblrs1050118
gopubmedrs1050118
geneviewrs1050118
scholarrs1050118
googlers1050118
pharmgkbrs1050118
gwascentralrs1050118
openSNPrs1050118
23andMers1050118
23andMe allrs1050118
SNP Nexus

SNPshotrs1050118
SNPdbers1050118
MSV3drs1050118
GWAS Ctlgrs1050118
Max Magnitude0
ClinVar
Risk rs1050118(A;A)
Alt rs1050118(A;A)
Reference rs1050118(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237776C>T
CLNSRC
CLNACC