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rs281860476

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860476(A;T)
Make rs281860476(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271255
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860476
ebirs281860476
HLIrs281860476
Exacrs281860476
Varsomers281860476
Maprs281860476
PheGenIrs281860476
hapmaprs281860476
1000 genomesrs281860476
hgdprs281860476
ensemblrs281860476
gopubmedrs281860476
geneviewrs281860476
scholarrs281860476
googlers281860476
pharmgkbrs281860476
gwascentralrs281860476
openSNPrs281860476
23andMers281860476
23andMe allrs281860476
SNP Nexus

SNPshotrs281860476
SNPdbers281860476
MSV3drs281860476
GWAS Ctlgrs281860476
Max Magnitude0
ClinVar
Risk rs281860476(T;T)
Alt rs281860476(T;T)
Reference rs281860476(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239032T>A
CLNSRC
CLNACC