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rs281860453

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860453(A;A)
Make rs281860453(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271314
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860453
ebirs281860453
HLIrs281860453
Exacrs281860453
Varsomers281860453
Maprs281860453
PheGenIrs281860453
hapmaprs281860453
1000 genomesrs281860453
hgdprs281860453
ensemblrs281860453
gopubmedrs281860453
geneviewrs281860453
scholarrs281860453
googlers281860453
pharmgkbrs281860453
gwascentralrs281860453
openSNPrs281860453
23andMers281860453
23andMe allrs281860453
SNP Nexus

SNPshotrs281860453
SNPdbers281860453
MSV3drs281860453
GWAS Ctlgrs281860453
Max Magnitude0
ClinVar
Risk rs281860453(A;A)
Alt rs281860453(A;A)
Reference rs281860453(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239091G>T
CLNSRC
CLNACC