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rs281864733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864733(C;T)
Make rs281864733(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942866
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864733
ebirs281864733
HLIrs281864733
Exacrs281864733
Varsomers281864733
Maprs281864733
PheGenIrs281864733
hapmaprs281864733
1000 genomesrs281864733
hgdprs281864733
ensemblrs281864733
gopubmedrs281864733
geneviewrs281864733
scholarrs281864733
googlers281864733
pharmgkbrs281864733
gwascentralrs281864733
openSNPrs281864733
23andMers281864733
23andMe allrs281864733
SNP Nexus

SNPshotrs281864733
SNPdbers281864733
MSV3drs281864733
GWAS Ctlgrs281864733
Max Magnitude0
ClinVar
Risk rs281864733(T;T)
Alt rs281864733(T;T)
Reference rs281864733(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910643C>T
CLNSRC
CLNACC