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rs281860535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860535(C;C)
Make rs281860535(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271117
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860535
ebirs281860535
HLIrs281860535
Exacrs281860535
Varsomers281860535
Maprs281860535
PheGenIrs281860535
hapmaprs281860535
1000 genomesrs281860535
hgdprs281860535
ensemblrs281860535
gopubmedrs281860535
geneviewrs281860535
scholarrs281860535
googlers281860535
pharmgkbrs281860535
gwascentralrs281860535
openSNPrs281860535
23andMers281860535
23andMe allrs281860535
SNP Nexus

SNPshotrs281860535
SNPdbers281860535
MSV3drs281860535
GWAS Ctlgrs281860535
Max Magnitude0
ClinVar
Risk rs281860535(C;C)
Alt rs281860535(C;C)
Reference rs281860535(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238894A>G
CLNSRC
CLNACC