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rs281860405

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860405(A;A)
Make rs281860405(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271659
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860405
ebirs281860405
HLIrs281860405
Exacrs281860405
Varsomers281860405
Maprs281860405
PheGenIrs281860405
hapmaprs281860405
1000 genomesrs281860405
hgdprs281860405
ensemblrs281860405
gopubmedrs281860405
geneviewrs281860405
scholarrs281860405
googlers281860405
pharmgkbrs281860405
gwascentralrs281860405
openSNPrs281860405
23andMers281860405
23andMe allrs281860405
SNP Nexus

SNPshotrs281860405
SNPdbers281860405
MSV3drs281860405
GWAS Ctlgrs281860405
Max Magnitude0
ClinVar
Risk rs281860405(A,T;A,T)
Alt rs281860405(A,T;A,T)
Reference rs281860405(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239436C>A; NC_000006.11:g.31239436C>T
CLNSRC
CLNACC