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rs1065600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1065600(A;A)
Make rs1065600(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270058
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1065600
ebirs1065600
HLIrs1065600
Exacrs1065600
Varsomers1065600
Maprs1065600
PheGenIrs1065600
hapmaprs1065600
1000 genomesrs1065600
hgdprs1065600
ensemblrs1065600
gopubmedrs1065600
geneviewrs1065600
scholarrs1065600
googlers1065600
pharmgkbrs1065600
gwascentralrs1065600
openSNPrs1065600
23andMers1065600
23andMe allrs1065600
SNP Nexus

SNPshotrs1065600
SNPdbers1065600
MSV3drs1065600
GWAS Ctlgrs1065600
GMAF0.02066
Max Magnitude0
ClinVar
Risk rs1065600(A;A)
Alt rs1065600(A;A)
Reference rs1065600(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237835A>T
CLNSRC
CLNACC