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rs281860529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860529(A;A)
Make rs281860529(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271126
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860529
ebirs281860529
HLIrs281860529
Exacrs281860529
Varsomers281860529
Maprs281860529
PheGenIrs281860529
hapmaprs281860529
1000 genomesrs281860529
hgdprs281860529
ensemblrs281860529
gopubmedrs281860529
geneviewrs281860529
scholarrs281860529
googlers281860529
pharmgkbrs281860529
gwascentralrs281860529
openSNPrs281860529
23andMers281860529
23andMe allrs281860529
SNP Nexus

SNPshotrs281860529
SNPdbers281860529
MSV3drs281860529
GWAS Ctlgrs281860529
Max Magnitude0
ClinVar
Risk rs281860529(A;A)
Alt rs281860529(A;A)
Reference rs281860529(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238903A>T
CLNSRC
CLNACC