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rs281864729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864729(G;G)
Make rs281864729(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942820
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864729
dbSNP (classic)rs281864729
ClinGenrs281864729
ebirs281864729
HLIrs281864729
Exacrs281864729
Gnomadrs281864729
Varsomers281864729
LitVarrs281864729
Maprs281864729
PheGenIrs281864729
Biobankrs281864729
1000 genomesrs281864729
hgdprs281864729
ensemblrs281864729
geneviewrs281864729
scholarrs281864729
googlers281864729
pharmgkbrs281864729
gwascentralrs281864729
openSNPrs281864729
23andMers281864729
SNPshotrs281864729
SNPdbers281864729
MSV3drs281864729
GWAS Ctlgrs281864729
Max Magnitude0
ClinVar
Risk rs281864729(G;G)
Alt rs281864729(G;G)
Reference Rs281864729(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910597T>G
CLNSRC
CLNACC