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rs281860451

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860451(A;A)
Make rs281860451(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271319
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860451
ebirs281860451
HLIrs281860451
Exacrs281860451
Varsomers281860451
Maprs281860451
PheGenIrs281860451
hapmaprs281860451
1000 genomesrs281860451
hgdprs281860451
ensemblrs281860451
gopubmedrs281860451
geneviewrs281860451
scholarrs281860451
googlers281860451
pharmgkbrs281860451
gwascentralrs281860451
openSNPrs281860451
23andMers281860451
23andMe allrs281860451
SNP Nexus

SNPshotrs281860451
SNPdbers281860451
MSV3drs281860451
GWAS Ctlgrs281860451
Max Magnitude0
ClinVar
Risk rs281860451(A;A)
Alt rs281860451(A;A)
Reference rs281860451(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239096A>T
CLNSRC
CLNACC