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rs281860559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860559(C;G)
Make rs281860559(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270390
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860559
ebirs281860559
HLIrs281860559
Exacrs281860559
Varsomers281860559
Maprs281860559
PheGenIrs281860559
hapmaprs281860559
1000 genomesrs281860559
hgdprs281860559
ensemblrs281860559
gopubmedrs281860559
geneviewrs281860559
scholarrs281860559
googlers281860559
pharmgkbrs281860559
gwascentralrs281860559
openSNPrs281860559
23andMers281860559
23andMe allrs281860559
SNP Nexus

SNPshotrs281860559
SNPdbers281860559
MSV3drs281860559
GWAS Ctlgrs281860559
Max Magnitude0
ClinVar
Risk rs281860559(G;G)
Alt rs281860559(G;G)
Reference rs281860559(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238167G>C
CLNSRC
CLNACC