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rs281860477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860477(C;C)
Make rs281860477(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271253
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860477
ebirs281860477
HLIrs281860477
Exacrs281860477
Varsomers281860477
Maprs281860477
PheGenIrs281860477
hapmaprs281860477
1000 genomesrs281860477
hgdprs281860477
ensemblrs281860477
gopubmedrs281860477
geneviewrs281860477
scholarrs281860477
googlers281860477
pharmgkbrs281860477
gwascentralrs281860477
openSNPrs281860477
23andMers281860477
23andMe allrs281860477
SNP Nexus

SNPshotrs281860477
SNPdbers281860477
MSV3drs281860477
GWAS Ctlgrs281860477
Max Magnitude0
ClinVar
Risk rs281860477(C;C)
Alt rs281860477(C;C)
Reference rs281860477(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239030A>G
CLNSRC
CLNACC