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rs281864732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864732(A;A)
Make rs281864732(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942856
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864732
ebirs281864732
HLIrs281864732
Exacrs281864732
Varsomers281864732
Maprs281864732
PheGenIrs281864732
hapmaprs281864732
1000 genomesrs281864732
hgdprs281864732
ensemblrs281864732
gopubmedrs281864732
geneviewrs281864732
scholarrs281864732
googlers281864732
pharmgkbrs281864732
gwascentralrs281864732
openSNPrs281864732
23andMers281864732
23andMe allrs281864732
SNP Nexus

SNPshotrs281864732
SNPdbers281864732
MSV3drs281864732
GWAS Ctlgrs281864732
Max Magnitude0
ClinVar
Risk rs281864732(A;A)
Alt rs281864732(A;A)
Reference rs281864732(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910633T>A
CLNSRC
CLNACC