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rs281860579

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860579(G;T)
Make rs281860579(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270084
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860579
ebirs281860579
HLIrs281860579
Exacrs281860579
Varsomers281860579
Maprs281860579
PheGenIrs281860579
hapmaprs281860579
1000 genomesrs281860579
hgdprs281860579
ensemblrs281860579
gopubmedrs281860579
geneviewrs281860579
scholarrs281860579
googlers281860579
pharmgkbrs281860579
gwascentralrs281860579
openSNPrs281860579
23andMers281860579
23andMe allrs281860579
SNP Nexus

SNPshotrs281860579
SNPdbers281860579
MSV3drs281860579
GWAS Ctlgrs281860579
Max Magnitude0
ClinVar
Risk rs281860579(T;T)
Alt rs281860579(T;T)
Reference rs281860579(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237861C>A
CLNSRC
CLNACC