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rs281864752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864752(C;T)
Make rs281864752(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943324
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864752
ebirs281864752
HLIrs281864752
Exacrs281864752
Varsomers281864752
Maprs281864752
PheGenIrs281864752
hapmaprs281864752
1000 genomesrs281864752
hgdprs281864752
ensemblrs281864752
gopubmedrs281864752
geneviewrs281864752
scholarrs281864752
googlers281864752
pharmgkbrs281864752
gwascentralrs281864752
openSNPrs281864752
23andMers281864752
23andMe allrs281864752
SNP Nexus

SNPshotrs281864752
SNPdbers281864752
MSV3drs281864752
GWAS Ctlgrs281864752
Max Magnitude0
ClinVar
Risk rs281864752(T;T)
Alt rs281864752(T;T)
Reference rs281864752(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911101C>T
CLNSRC
CLNACC