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rs281860490

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860490(A;A)
Make rs281860490(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271227
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860490
ebirs281860490
HLIrs281860490
Exacrs281860490
Varsomers281860490
Maprs281860490
PheGenIrs281860490
hapmaprs281860490
1000 genomesrs281860490
hgdprs281860490
ensemblrs281860490
gopubmedrs281860490
geneviewrs281860490
scholarrs281860490
googlers281860490
pharmgkbrs281860490
gwascentralrs281860490
openSNPrs281860490
23andMers281860490
23andMe allrs281860490
SNP Nexus

SNPshotrs281860490
SNPdbers281860490
MSV3drs281860490
GWAS Ctlgrs281860490
Max Magnitude0
ClinVar
Risk rs281860490(A;A)
Alt rs281860490(A;A)
Reference rs281860490(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239004G>T
CLNSRC
CLNACC