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rs281860435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860435(A;A)
Make rs281860435(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271602
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860435
ebirs281860435
HLIrs281860435
Exacrs281860435
Varsomers281860435
Maprs281860435
PheGenIrs281860435
hapmaprs281860435
1000 genomesrs281860435
hgdprs281860435
ensemblrs281860435
gopubmedrs281860435
geneviewrs281860435
scholarrs281860435
googlers281860435
pharmgkbrs281860435
gwascentralrs281860435
openSNPrs281860435
23andMers281860435
23andMe allrs281860435
SNP Nexus

SNPshotrs281860435
SNPdbers281860435
MSV3drs281860435
GWAS Ctlgrs281860435
Max Magnitude0
ClinVar
Risk rs281860435(A,T;A,T)
Alt rs281860435(A,T;A,T)
Reference rs281860435(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239379C>A; NC_000006.11:g.31239379C>T
CLNSRC
CLNACC