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rs281860531

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860531(C;C)
Make rs281860531(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271124
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860531
ebirs281860531
HLIrs281860531
Exacrs281860531
Varsomers281860531
Maprs281860531
PheGenIrs281860531
hapmaprs281860531
1000 genomesrs281860531
hgdprs281860531
ensemblrs281860531
gopubmedrs281860531
geneviewrs281860531
scholarrs281860531
googlers281860531
pharmgkbrs281860531
gwascentralrs281860531
openSNPrs281860531
23andMers281860531
23andMe allrs281860531
SNP Nexus

SNPshotrs281860531
SNPdbers281860531
MSV3drs281860531
GWAS Ctlgrs281860531
Max Magnitude0
ClinVar
Risk rs281860531(C;C)
Alt rs281860531(C;C)
Reference rs281860531(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238901C>G
CLNSRC
CLNACC