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

rs281864766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864766(C;T)
Make rs281864766(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944203
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864766
ebirs281864766
HLIrs281864766
Exacrs281864766
Varsomers281864766
Maprs281864766
PheGenIrs281864766
hapmaprs281864766
1000 genomesrs281864766
hgdprs281864766
ensemblrs281864766
gopubmedrs281864766
geneviewrs281864766
scholarrs281864766
googlers281864766
pharmgkbrs281864766
gwascentralrs281864766
openSNPrs281864766
23andMers281864766
23andMe allrs281864766
SNP Nexus

SNPshotrs281864766
SNPdbers281864766
MSV3drs281864766
GWAS Ctlgrs281864766
Max Magnitude0
ClinVar
Risk rs281864766(T;T)
Alt rs281864766(T;T)
Reference rs281864766(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911980C>T
CLNSRC
CLNACC