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rs281860489

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860489(A;A)
Make rs281860489(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271228
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860489
ebirs281860489
HLIrs281860489
Exacrs281860489
Varsomers281860489
Maprs281860489
PheGenIrs281860489
hapmaprs281860489
1000 genomesrs281860489
hgdprs281860489
ensemblrs281860489
gopubmedrs281860489
geneviewrs281860489
scholarrs281860489
googlers281860489
pharmgkbrs281860489
gwascentralrs281860489
openSNPrs281860489
23andMers281860489
23andMe allrs281860489
SNP Nexus

SNPshotrs281860489
SNPdbers281860489
MSV3drs281860489
GWAS Ctlgrs281860489
Max Magnitude0
ClinVar
Risk rs281860489(A,C,T;A,C,T)
Alt rs281860489(A,C,T;A,C,T)
Reference rs281860489(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239005C>A; NC_000006.11:g.31239005C>G; NC_000006.11:g.31239005C>T
CLNSRC
CLNACC