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rs281860446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860446(A;G)
Make rs281860446(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271328
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860446
ebirs281860446
HLIrs281860446
Exacrs281860446
Varsomers281860446
Maprs281860446
PheGenIrs281860446
hapmaprs281860446
1000 genomesrs281860446
hgdprs281860446
ensemblrs281860446
gopubmedrs281860446
geneviewrs281860446
scholarrs281860446
googlers281860446
pharmgkbrs281860446
gwascentralrs281860446
openSNPrs281860446
23andMers281860446
23andMe allrs281860446
SNP Nexus

SNPshotrs281860446
SNPdbers281860446
MSV3drs281860446
GWAS Ctlgrs281860446
Max Magnitude0
ClinVar
Risk rs281860446(G,T;G,T)
Alt rs281860446(G,T;G,T)
Reference rs281860446(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239105T>A; NC_000006.11:g.31239105T>C
CLNSRC
CLNACC