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rs281864754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864754(C;G)
Make rs281864754(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943424
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864754
ebirs281864754
HLIrs281864754
Exacrs281864754
Varsomers281864754
Maprs281864754
PheGenIrs281864754
hapmaprs281864754
1000 genomesrs281864754
hgdprs281864754
ensemblrs281864754
gopubmedrs281864754
geneviewrs281864754
scholarrs281864754
googlers281864754
pharmgkbrs281864754
gwascentralrs281864754
openSNPrs281864754
23andMers281864754
23andMe allrs281864754
SNP Nexus

SNPshotrs281864754
SNPdbers281864754
MSV3drs281864754
GWAS Ctlgrs281864754
Max Magnitude0
ClinVar
Risk rs281864754(G,T;G,T)
Alt rs281864754(G,T;G,T)
Reference rs281864754(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911201C>G; NC_000006.11:g.29911201C>T
CLNSRC
CLNACC