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rs281860533

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860533(-;-)
Make rs281860533(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271122
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860533
ebirs281860533
HLIrs281860533
Exacrs281860533
Varsomers281860533
Maprs281860533
PheGenIrs281860533
hapmaprs281860533
1000 genomesrs281860533
hgdprs281860533
ensemblrs281860533
gopubmedrs281860533
geneviewrs281860533
scholarrs281860533
googlers281860533
pharmgkbrs281860533
gwascentralrs281860533
openSNPrs281860533
23andMers281860533
23andMe allrs281860533
SNP Nexus

SNPshotrs281860533
SNPdbers281860533
MSV3drs281860533
GWAS Ctlgrs281860533
Max Magnitude0
ClinVar
Risk rs281860533(;)
Alt rs281860533(;)
Reference rs281860533(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238899delC
CLNSRC
CLNACC