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rs281864758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864758(A;A)
Make rs281864758(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943509
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864758
dbSNP (classic)rs281864758
ClinGenrs281864758
ebirs281864758
HLIrs281864758
Exacrs281864758
Gnomadrs281864758
Varsomers281864758
LitVarrs281864758
Maprs281864758
PheGenIrs281864758
Biobankrs281864758
1000 genomesrs281864758
hgdprs281864758
ensemblrs281864758
geneviewrs281864758
scholarrs281864758
googlers281864758
pharmgkbrs281864758
gwascentralrs281864758
openSNPrs281864758
23andMers281864758
SNPshotrs281864758
SNPdbers281864758
MSV3drs281864758
GWAS Ctlgrs281864758
Max Magnitude0
ClinVar
Risk rs281864758(A;A)
Alt rs281864758(A;A)
Reference Rs281864758(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911286C>A
CLNSRC
CLNACC