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rs281864760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864760(C;C)
Make rs281864760(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943532
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864760
ebirs281864760
HLIrs281864760
Exacrs281864760
Varsomers281864760
Maprs281864760
PheGenIrs281864760
hapmaprs281864760
1000 genomesrs281864760
hgdprs281864760
ensemblrs281864760
gopubmedrs281864760
geneviewrs281864760
scholarrs281864760
googlers281864760
pharmgkbrs281864760
gwascentralrs281864760
openSNPrs281864760
23andMers281864760
23andMe allrs281864760
SNP Nexus

SNPshotrs281864760
SNPdbers281864760
MSV3drs281864760
GWAS Ctlgrs281864760
Max Magnitude0
ClinVar
Risk rs281864760(C;C)
Alt rs281864760(C;C)
Reference rs281864760(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911309T>C
CLNSRC
CLNACC