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rs281860558

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860558(C;G)
Make rs281860558(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270401
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860558
ebirs281860558
HLIrs281860558
Exacrs281860558
Varsomers281860558
Maprs281860558
PheGenIrs281860558
hapmaprs281860558
1000 genomesrs281860558
hgdprs281860558
ensemblrs281860558
gopubmedrs281860558
geneviewrs281860558
scholarrs281860558
googlers281860558
pharmgkbrs281860558
gwascentralrs281860558
openSNPrs281860558
23andMers281860558
23andMe allrs281860558
SNP Nexus

SNPshotrs281860558
SNPdbers281860558
MSV3drs281860558
GWAS Ctlgrs281860558
Max Magnitude0
ClinVar
Risk rs281860558(G,T;G,T)
Alt rs281860558(G,T;G,T)
Reference rs281860558(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238178G>A; NC_000006.11:g.31238178G>C
CLNSRC
CLNACC