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rs281860552

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860552(C;C)
Make rs281860552(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270447
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860552
ebirs281860552
HLIrs281860552
Exacrs281860552
Varsomers281860552
Maprs281860552
PheGenIrs281860552
hapmaprs281860552
1000 genomesrs281860552
hgdprs281860552
ensemblrs281860552
gopubmedrs281860552
geneviewrs281860552
scholarrs281860552
googlers281860552
pharmgkbrs281860552
gwascentralrs281860552
openSNPrs281860552
23andMers281860552
23andMe allrs281860552
SNP Nexus

SNPshotrs281860552
SNPdbers281860552
MSV3drs281860552
GWAS Ctlgrs281860552
Max Magnitude0
ClinVar
Risk rs281860552(C;C)
Alt rs281860552(C;C)
Reference rs281860552(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238224C>G
CLNSRC
CLNACC