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rs1065711

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1065711(C;T)
Make rs1065711(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269076
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1065711
ebirs1065711
HLIrs1065711
Exacrs1065711
Varsomers1065711
Maprs1065711
PheGenIrs1065711
hapmaprs1065711
1000 genomesrs1065711
hgdprs1065711
ensemblrs1065711
gopubmedrs1065711
geneviewrs1065711
scholarrs1065711
googlers1065711
pharmgkbrs1065711
gwascentralrs1065711
openSNPrs1065711
23andMers1065711
23andMe allrs1065711
SNP Nexus

SNPshotrs1065711
SNPdbers1065711
MSV3drs1065711
GWAS Ctlgrs1065711
GMAF0.1304
Max Magnitude0
ClinVar
Risk rs1065711(T;T)
Alt rs1065711(T;T)
Reference rs1065711(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236853G; NC_000006.11:g.31236853G>A
CLNSRC
CLNACC