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rs281864759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281864759(A;G)
Make rs281864759(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943517
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864759
ebirs281864759
HLIrs281864759
Exacrs281864759
Varsomers281864759
Maprs281864759
PheGenIrs281864759
hapmaprs281864759
1000 genomesrs281864759
hgdprs281864759
ensemblrs281864759
gopubmedrs281864759
geneviewrs281864759
scholarrs281864759
googlers281864759
pharmgkbrs281864759
gwascentralrs281864759
openSNPrs281864759
23andMers281864759
23andMe allrs281864759
SNP Nexus

SNPshotrs281864759
SNPdbers281864759
MSV3drs281864759
GWAS Ctlgrs281864759
Max Magnitude0
ClinVar
Risk rs281864759(G;G)
Alt rs281864759(G;G)
Reference Rs281864759(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911294A>G
CLNSRC
CLNACC