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rs281860459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860459(A;A)
Make rs281860459(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271299
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860459
ebirs281860459
HLIrs281860459
Exacrs281860459
Varsomers281860459
Maprs281860459
PheGenIrs281860459
hapmaprs281860459
1000 genomesrs281860459
hgdprs281860459
ensemblrs281860459
gopubmedrs281860459
geneviewrs281860459
scholarrs281860459
googlers281860459
pharmgkbrs281860459
gwascentralrs281860459
openSNPrs281860459
23andMers281860459
23andMe allrs281860459
SNP Nexus

SNPshotrs281860459
SNPdbers281860459
MSV3drs281860459
GWAS Ctlgrs281860459
Max Magnitude0
ClinVar
Risk rs281860459(A,C;A,C)
Alt rs281860459(A,C;A,C)
Reference rs281860459(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239076C>G; NC_000006.11:g.31239076C>T
CLNSRC
CLNACC