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rs281860452

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860452(A;A)
Make rs281860452(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271317
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860452
ebirs281860452
HLIrs281860452
Exacrs281860452
Varsomers281860452
Maprs281860452
PheGenIrs281860452
hapmaprs281860452
1000 genomesrs281860452
hgdprs281860452
ensemblrs281860452
gopubmedrs281860452
geneviewrs281860452
scholarrs281860452
googlers281860452
pharmgkbrs281860452
gwascentralrs281860452
openSNPrs281860452
23andMers281860452
23andMe allrs281860452
SNP Nexus

SNPshotrs281860452
SNPdbers281860452
MSV3drs281860452
GWAS Ctlgrs281860452
Max Magnitude0
ClinVar
Risk rs281860452(A,T;A,T)
Alt rs281860452(A,T;A,T)
Reference rs281860452(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239094G>A; NC_000006.11:g.31239094G>T
CLNSRC
CLNACC