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rs281860493

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860493(C;T)
Make rs281860493(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271216
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860493
ebirs281860493
HLIrs281860493
Exacrs281860493
Varsomers281860493
Maprs281860493
PheGenIrs281860493
hapmaprs281860493
1000 genomesrs281860493
hgdprs281860493
ensemblrs281860493
gopubmedrs281860493
geneviewrs281860493
scholarrs281860493
googlers281860493
pharmgkbrs281860493
gwascentralrs281860493
openSNPrs281860493
23andMers281860493
23andMe allrs281860493
SNP Nexus

SNPshotrs281860493
SNPdbers281860493
MSV3drs281860493
GWAS Ctlgrs281860493
Max Magnitude0
ClinVar
Risk rs281860493(T;T)
Alt rs281860493(T;T)
Reference rs281860493(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238993G>A
CLNSRC
CLNACC