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rs281864769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281864769(A;C)
Make rs281864769(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944344
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864769
ebirs281864769
HLIrs281864769
Exacrs281864769
Varsomers281864769
Maprs281864769
PheGenIrs281864769
hapmaprs281864769
1000 genomesrs281864769
hgdprs281864769
ensemblrs281864769
gopubmedrs281864769
geneviewrs281864769
scholarrs281864769
googlers281864769
pharmgkbrs281864769
gwascentralrs281864769
openSNPrs281864769
23andMers281864769
23andMe allrs281864769
SNP Nexus

SNPshotrs281864769
SNPdbers281864769
MSV3drs281864769
GWAS Ctlgrs281864769
Max Magnitude0
ClinVar
Risk rs281864769(C;C)
Alt rs281864769(C;C)
Reference rs281864769(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912121A>C
CLNSRC
CLNACC