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rs281864722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864722(C;C)
Make rs281864722(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942759
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864722
ebirs281864722
HLIrs281864722
Exacrs281864722
Varsomers281864722
Maprs281864722
PheGenIrs281864722
hapmaprs281864722
1000 genomesrs281864722
hgdprs281864722
ensemblrs281864722
gopubmedrs281864722
geneviewrs281864722
scholarrs281864722
googlers281864722
pharmgkbrs281864722
gwascentralrs281864722
openSNPrs281864722
23andMers281864722
23andMe allrs281864722
SNP Nexus

SNPshotrs281864722
SNPdbers281864722
MSV3drs281864722
GWAS Ctlgrs281864722
Max Magnitude0
ClinVar
Risk rs281864722(C;C)
Alt rs281864722(C;C)
Reference rs281864722(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910536T>C
CLNSRC
CLNACC