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rs281860462

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860462(C;G)
Make rs281860462(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271292
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860462
ebirs281860462
HLIrs281860462
Exacrs281860462
Varsomers281860462
Maprs281860462
PheGenIrs281860462
hapmaprs281860462
1000 genomesrs281860462
hgdprs281860462
ensemblrs281860462
gopubmedrs281860462
geneviewrs281860462
scholarrs281860462
googlers281860462
pharmgkbrs281860462
gwascentralrs281860462
openSNPrs281860462
23andMers281860462
23andMe allrs281860462
SNP Nexus

SNPshotrs281860462
SNPdbers281860462
MSV3drs281860462
GWAS Ctlgrs281860462
Max Magnitude0
ClinVar
Risk rs281860462(G,T;G,T)
Alt rs281860462(G,T;G,T)
Reference rs281860462(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239069G>A; NC_000006.11:g.31239069G>C
CLNSRC
CLNACC