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rs281864770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281864770(A;A)
Make rs281864770(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944364
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864770
dbSNP (classic)rs281864770
ClinGenrs281864770
ebirs281864770
HLIrs281864770
Exacrs281864770
Gnomadrs281864770
Varsomers281864770
LitVarrs281864770
Maprs281864770
PheGenIrs281864770
Biobankrs281864770
1000 genomesrs281864770
hgdprs281864770
ensemblrs281864770
geneviewrs281864770
scholarrs281864770
googlers281864770
pharmgkbrs281864770
gwascentralrs281864770
openSNPrs281864770
23andMers281864770
SNPshotrs281864770
SNPdbers281864770
MSV3drs281864770
GWAS Ctlgrs281864770
Max Magnitude0
ClinVar
Risk rs281864770(A;A)
Alt rs281864770(A;A)
Reference Rs281864770(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912141G>A
CLNSRC
CLNACC