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rs281860460

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860460(A;A)
Make rs281860460(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271298
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860460
ebirs281860460
HLIrs281860460
Exacrs281860460
Varsomers281860460
Maprs281860460
PheGenIrs281860460
hapmaprs281860460
1000 genomesrs281860460
hgdprs281860460
ensemblrs281860460
gopubmedrs281860460
geneviewrs281860460
scholarrs281860460
googlers281860460
pharmgkbrs281860460
gwascentralrs281860460
openSNPrs281860460
23andMers281860460
23andMe allrs281860460
SNP Nexus

SNPshotrs281860460
SNPdbers281860460
MSV3drs281860460
GWAS Ctlgrs281860460
Max Magnitude0
ClinVar
Risk rs281860460(A,G,T;A,G,T)
Alt rs281860460(A,G,T;A,G,T)
Reference rs281860460(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239075G>A; NC_000006.11:g.31239075G>C; NC_000006.11:g.31239075G>T
CLNSRC
CLNACC