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rs281860468

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860468(C;T)
Make rs281860468(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271277
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860468
ebirs281860468
HLIrs281860468
Exacrs281860468
Varsomers281860468
Maprs281860468
PheGenIrs281860468
hapmaprs281860468
1000 genomesrs281860468
hgdprs281860468
ensemblrs281860468
gopubmedrs281860468
geneviewrs281860468
scholarrs281860468
googlers281860468
pharmgkbrs281860468
gwascentralrs281860468
openSNPrs281860468
23andMers281860468
23andMe allrs281860468
SNP Nexus

SNPshotrs281860468
SNPdbers281860468
MSV3drs281860468
GWAS Ctlgrs281860468
Max Magnitude0
ClinVar
Risk rs281860468(T;T)
Alt rs281860468(T;T)
Reference rs281860468(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239054G>A
CLNSRC
CLNACC