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rs281860582

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860582(G;G)
Make rs281860582(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270080
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860582
ebirs281860582
HLIrs281860582
Exacrs281860582
Varsomers281860582
Maprs281860582
PheGenIrs281860582
hapmaprs281860582
1000 genomesrs281860582
hgdprs281860582
ensemblrs281860582
gopubmedrs281860582
geneviewrs281860582
scholarrs281860582
googlers281860582
pharmgkbrs281860582
gwascentralrs281860582
openSNPrs281860582
23andMers281860582
23andMe allrs281860582
SNP Nexus

SNPshotrs281860582
SNPdbers281860582
MSV3drs281860582
GWAS Ctlgrs281860582
Max Magnitude0
ClinVar
Risk rs281860582(G;G)
Alt rs281860582(G;G)
Reference rs281860582(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237857A>C
CLNSRC
CLNACC