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rs281860466

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860466(C;T)
Make rs281860466(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271287
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860466
ebirs281860466
HLIrs281860466
Exacrs281860466
Varsomers281860466
Maprs281860466
PheGenIrs281860466
hapmaprs281860466
1000 genomesrs281860466
hgdprs281860466
ensemblrs281860466
gopubmedrs281860466
geneviewrs281860466
scholarrs281860466
googlers281860466
pharmgkbrs281860466
gwascentralrs281860466
openSNPrs281860466
23andMers281860466
23andMe allrs281860466
SNP Nexus

SNPshotrs281860466
SNPdbers281860466
MSV3drs281860466
GWAS Ctlgrs281860466
Max Magnitude0
ClinVar
Risk rs281860466(T;T)
Alt rs281860466(T;T)
Reference rs281860466(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239064G>A
CLNSRC
CLNACC