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rs281860406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860406(C;T)
Make rs281860406(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271658
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860406
ebirs281860406
HLIrs281860406
Exacrs281860406
Varsomers281860406
Maprs281860406
PheGenIrs281860406
hapmaprs281860406
1000 genomesrs281860406
hgdprs281860406
ensemblrs281860406
gopubmedrs281860406
geneviewrs281860406
scholarrs281860406
googlers281860406
pharmgkbrs281860406
gwascentralrs281860406
openSNPrs281860406
23andMers281860406
23andMe allrs281860406
SNP Nexus

SNPshotrs281860406
SNPdbers281860406
MSV3drs281860406
GWAS Ctlgrs281860406
Max Magnitude0
ClinVar
Risk rs281860406(T;T)
Alt rs281860406(T;T)
Reference rs281860406(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239435G>A
CLNSRC
CLNACC