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rs281860467

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860467(A;A)
Make rs281860467(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271278
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860467
ebirs281860467
HLIrs281860467
Exacrs281860467
Varsomers281860467
Maprs281860467
PheGenIrs281860467
hapmaprs281860467
1000 genomesrs281860467
hgdprs281860467
ensemblrs281860467
gopubmedrs281860467
geneviewrs281860467
scholarrs281860467
googlers281860467
pharmgkbrs281860467
gwascentralrs281860467
openSNPrs281860467
23andMers281860467
23andMe allrs281860467
SNP Nexus

SNPshotrs281860467
SNPdbers281860467
MSV3drs281860467
GWAS Ctlgrs281860467
Max Magnitude0
ClinVar
Risk rs281860467(A,G,T;A,G,T)
Alt rs281860467(A,G,T;A,G,T)
Reference rs281860467(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239055G>A; NC_000006.11:g.31239055G>C; NC_000006.11:g.31239055G>T
CLNSRC
CLNACC