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rs281860581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860581(A;A)
Make rs281860581(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270082
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860581
ebirs281860581
HLIrs281860581
Exacrs281860581
Varsomers281860581
Maprs281860581
PheGenIrs281860581
hapmaprs281860581
1000 genomesrs281860581
hgdprs281860581
ensemblrs281860581
gopubmedrs281860581
geneviewrs281860581
scholarrs281860581
googlers281860581
pharmgkbrs281860581
gwascentralrs281860581
openSNPrs281860581
23andMers281860581
23andMe allrs281860581
SNP Nexus

SNPshotrs281860581
SNPdbers281860581
MSV3drs281860581
GWAS Ctlgrs281860581
Max Magnitude0
ClinVar
Risk rs281860581(A;A)
Alt rs281860581(A;A)
Reference rs281860581(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237859G>T
CLNSRC
CLNACC