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rs281860506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860506(C;C)
Make rs281860506(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271182
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860506
ebirs281860506
HLIrs281860506
Exacrs281860506
Varsomers281860506
Maprs281860506
PheGenIrs281860506
hapmaprs281860506
1000 genomesrs281860506
hgdprs281860506
ensemblrs281860506
gopubmedrs281860506
geneviewrs281860506
scholarrs281860506
googlers281860506
pharmgkbrs281860506
gwascentralrs281860506
openSNPrs281860506
23andMers281860506
23andMe allrs281860506
SNP Nexus

SNPshotrs281860506
SNPdbers281860506
MSV3drs281860506
GWAS Ctlgrs281860506
Max Magnitude0
ClinVar
Risk rs281860506(C;C)
Alt rs281860506(C;C)
Reference rs281860506(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238959C>G
CLNSRC
CLNACC