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rs1050716

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050716(C;G)
Make rs1050716(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270453
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050716
ebirs1050716
HLIrs1050716
Exacrs1050716
Varsomers1050716
Maprs1050716
PheGenIrs1050716
hapmaprs1050716
1000 genomesrs1050716
hgdprs1050716
ensemblrs1050716
gopubmedrs1050716
geneviewrs1050716
scholarrs1050716
googlers1050716
pharmgkbrs1050716
gwascentralrs1050716
openSNPrs1050716
23andMers1050716
23andMe allrs1050716
SNP Nexus

SNPshotrs1050716
SNPdbers1050716
MSV3drs1050716
GWAS Ctlgrs1050716
GMAF0.225
Max Magnitude0
ClinVar
Risk rs1050716(A,G;A,G)
Alt rs1050716(A,G;A,G)
Reference rs1050716(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238230G>C; NC_000006.11:g.31238230G>T
CLNSRC
CLNACC