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rs281860399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860399(A;T)
Make rs281860399(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271676
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860399
ebirs281860399
HLIrs281860399
Exacrs281860399
Varsomers281860399
Maprs281860399
PheGenIrs281860399
hapmaprs281860399
1000 genomesrs281860399
hgdprs281860399
ensemblrs281860399
gopubmedrs281860399
geneviewrs281860399
scholarrs281860399
googlers281860399
pharmgkbrs281860399
gwascentralrs281860399
openSNPrs281860399
23andMers281860399
23andMe allrs281860399
SNP Nexus

SNPshotrs281860399
SNPdbers281860399
MSV3drs281860399
GWAS Ctlgrs281860399
Max Magnitude0
ClinVar
Risk rs281860399(T;T)
Alt rs281860399(T;T)
Reference rs281860399(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239453T>A
CLNSRC
CLNACC