Have questions? Visit https://www.reddit.com/r/SNPedia

rs281864736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864736(C;T)
Make rs281864736(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942915
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864736
ebirs281864736
HLIrs281864736
Exacrs281864736
Varsomers281864736
Maprs281864736
PheGenIrs281864736
hapmaprs281864736
1000 genomesrs281864736
hgdprs281864736
ensemblrs281864736
gopubmedrs281864736
geneviewrs281864736
scholarrs281864736
googlers281864736
pharmgkbrs281864736
gwascentralrs281864736
openSNPrs281864736
23andMers281864736
23andMe allrs281864736
SNP Nexus

SNPshotrs281864736
SNPdbers281864736
MSV3drs281864736
GWAS Ctlgrs281864736
Max Magnitude0
ClinVar
Risk rs281864736(T;T)
Alt rs281864736(T;T)
Reference rs281864736(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910692C>T
CLNSRC
CLNACC