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rs281860484

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860484(A;A)
Make rs281860484(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271238
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860484
ebirs281860484
HLIrs281860484
Exacrs281860484
Varsomers281860484
Maprs281860484
PheGenIrs281860484
hapmaprs281860484
1000 genomesrs281860484
hgdprs281860484
ensemblrs281860484
gopubmedrs281860484
geneviewrs281860484
scholarrs281860484
googlers281860484
pharmgkbrs281860484
gwascentralrs281860484
openSNPrs281860484
23andMers281860484
23andMe allrs281860484
SNP Nexus

SNPshotrs281860484
SNPdbers281860484
MSV3drs281860484
GWAS Ctlgrs281860484
Max Magnitude0
ClinVar
Risk rs281860484(A,C,T;A,C,T)
Alt rs281860484(A,C,T;A,C,T)
Reference rs281860484(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239015C>A; NC_000006.11:g.31239015C>G; NC_000006.11:g.31239015C>T
CLNSRC
CLNACC