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rs281860474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860474(A;G)
Make rs281860474(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271258
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860474
ebirs281860474
HLIrs281860474
Exacrs281860474
Varsomers281860474
Maprs281860474
PheGenIrs281860474
hapmaprs281860474
1000 genomesrs281860474
hgdprs281860474
ensemblrs281860474
gopubmedrs281860474
geneviewrs281860474
scholarrs281860474
googlers281860474
pharmgkbrs281860474
gwascentralrs281860474
openSNPrs281860474
23andMers281860474
23andMe allrs281860474
SNP Nexus

SNPshotrs281860474
SNPdbers281860474
MSV3drs281860474
GWAS Ctlgrs281860474
Max Magnitude0
ClinVar
Risk rs281860474(G,T;G,T)
Alt rs281860474(G,T;G,T)
Reference rs281860474(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239035T>A; NC_000006.11:g.31239035T>C
CLNSRC
CLNACC