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rs281864763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864763(C;C)
Make rs281864763(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944159
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864763
ebirs281864763
HLIrs281864763
Exacrs281864763
Varsomers281864763
Maprs281864763
PheGenIrs281864763
hapmaprs281864763
1000 genomesrs281864763
hgdprs281864763
ensemblrs281864763
gopubmedrs281864763
geneviewrs281864763
scholarrs281864763
googlers281864763
pharmgkbrs281864763
gwascentralrs281864763
openSNPrs281864763
23andMers281864763
23andMe allrs281864763
SNP Nexus

SNPshotrs281864763
SNPdbers281864763
MSV3drs281864763
GWAS Ctlgrs281864763
Max Magnitude0
ClinVar
Risk rs281864763(C;C)
Alt rs281864763(C;C)
Reference rs281864763(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911936T>C
CLNSRC
CLNACC