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rs281860589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860589(C;T)
Make rs281860589(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269423
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860589
ebirs281860589
HLIrs281860589
Exacrs281860589
Varsomers281860589
Maprs281860589
PheGenIrs281860589
hapmaprs281860589
1000 genomesrs281860589
hgdprs281860589
ensemblrs281860589
gopubmedrs281860589
geneviewrs281860589
scholarrs281860589
googlers281860589
pharmgkbrs281860589
gwascentralrs281860589
openSNPrs281860589
23andMers281860589
23andMe allrs281860589
SNP Nexus

SNPshotrs281860589
SNPdbers281860589
MSV3drs281860589
GWAS Ctlgrs281860589
Max Magnitude0
ClinVar
Risk rs281860589(T;T)
Alt rs281860589(T;T)
Reference Rs281860589(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237200G>A
CLNSRC
CLNACC