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rs281864772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864772(C;T)
Make rs281864772(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944384
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864772
ebirs281864772
HLIrs281864772
Exacrs281864772
Varsomers281864772
Maprs281864772
PheGenIrs281864772
hapmaprs281864772
1000 genomesrs281864772
hgdprs281864772
ensemblrs281864772
gopubmedrs281864772
geneviewrs281864772
scholarrs281864772
googlers281864772
pharmgkbrs281864772
gwascentralrs281864772
openSNPrs281864772
23andMers281864772
23andMe allrs281864772
SNP Nexus

SNPshotrs281864772
SNPdbers281864772
MSV3drs281864772
GWAS Ctlgrs281864772
Max Magnitude0
ClinVar
Risk rs281864772(T;T)
Alt rs281864772(T;T)
Reference rs281864772(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912161C>T
CLNSRC
CLNACC