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rs281860590

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860590(A;A)
Make rs281860590(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269407
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860590
ebirs281860590
HLIrs281860590
Exacrs281860590
Varsomers281860590
Maprs281860590
PheGenIrs281860590
hapmaprs281860590
1000 genomesrs281860590
hgdprs281860590
ensemblrs281860590
gopubmedrs281860590
geneviewrs281860590
scholarrs281860590
googlers281860590
pharmgkbrs281860590
gwascentralrs281860590
openSNPrs281860590
23andMers281860590
23andMe allrs281860590
SNP Nexus

SNPshotrs281860590
SNPdbers281860590
MSV3drs281860590
GWAS Ctlgrs281860590
Max Magnitude0
ClinVar
Risk rs281860590(A;A)
Alt rs281860590(A;A)
Reference rs281860590(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237184G>T
CLNSRC
CLNACC