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rs281860586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860586(-;-)
Make rs281860586(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269807
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860586
ebirs281860586
HLIrs281860586
Exacrs281860586
Varsomers281860586
Maprs281860586
PheGenIrs281860586
hapmaprs281860586
1000 genomesrs281860586
hgdprs281860586
ensemblrs281860586
gopubmedrs281860586
geneviewrs281860586
scholarrs281860586
googlers281860586
pharmgkbrs281860586
gwascentralrs281860586
openSNPrs281860586
23andMers281860586
23andMe allrs281860586
SNP Nexus

SNPshotrs281860586
SNPdbers281860586
MSV3drs281860586
GWAS Ctlgrs281860586
Max Magnitude0
ClinVar
Risk rs281860586(;)
Alt rs281860586(;)
Reference rs281860586(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237584delC
CLNSRC
CLNACC