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rs76798670

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs76798670(A;G)
Make rs76798670(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269455
GeneHLA-C
is asnp
is mentioned by
dbSNPrs76798670
ebirs76798670
HLIrs76798670
Exacrs76798670
Varsomers76798670
Maprs76798670
PheGenIrs76798670
hapmaprs76798670
1000 genomesrs76798670
hgdprs76798670
ensemblrs76798670
gopubmedrs76798670
geneviewrs76798670
scholarrs76798670
googlers76798670
pharmgkbrs76798670
gwascentralrs76798670
openSNPrs76798670
23andMers76798670
23andMe allrs76798670
SNP Nexus

SNPshotrs76798670
SNPdbers76798670
MSV3drs76798670
GWAS Ctlgrs76798670
Max Magnitude0
ClinVar
Risk rs76798670(G;G)
Alt rs76798670(G;G)
Reference rs76798670(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237232T>C
CLNSRC
CLNACC