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rs281860481

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860481(A;A)
Make rs281860481(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271247
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860481
ebirs281860481
HLIrs281860481
Exacrs281860481
Varsomers281860481
Maprs281860481
PheGenIrs281860481
hapmaprs281860481
1000 genomesrs281860481
hgdprs281860481
ensemblrs281860481
gopubmedrs281860481
geneviewrs281860481
scholarrs281860481
googlers281860481
pharmgkbrs281860481
gwascentralrs281860481
openSNPrs281860481
23andMers281860481
23andMe allrs281860481
SNP Nexus

SNPshotrs281860481
SNPdbers281860481
MSV3drs281860481
GWAS Ctlgrs281860481
Max Magnitude0
ClinVar
Risk rs281860481(A,T;A,T)
Alt rs281860481(A,T;A,T)
Reference rs281860481(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239024C>A; NC_000006.11:g.31239024C>T
CLNSRC
CLNACC