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rs281860563

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860563(C;T)
Make rs281860563(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270363
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860563
ebirs281860563
HLIrs281860563
Exacrs281860563
Varsomers281860563
Maprs281860563
PheGenIrs281860563
hapmaprs281860563
1000 genomesrs281860563
hgdprs281860563
ensemblrs281860563
gopubmedrs281860563
geneviewrs281860563
scholarrs281860563
googlers281860563
pharmgkbrs281860563
gwascentralrs281860563
openSNPrs281860563
23andMers281860563
23andMe allrs281860563
SNP Nexus

SNPshotrs281860563
SNPdbers281860563
MSV3drs281860563
GWAS Ctlgrs281860563
Max Magnitude0
ClinVar
Risk rs281860563(T;T)
Alt rs281860563(T;T)
Reference rs281860563(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238140G>A
CLNSRC
CLNACC