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rs281864730

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864730(A;A)
Make rs281864730(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942836
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864730
ebirs281864730
HLIrs281864730
Exacrs281864730
Varsomers281864730
Maprs281864730
PheGenIrs281864730
hapmaprs281864730
1000 genomesrs281864730
hgdprs281864730
ensemblrs281864730
gopubmedrs281864730
geneviewrs281864730
scholarrs281864730
googlers281864730
pharmgkbrs281864730
gwascentralrs281864730
openSNPrs281864730
23andMers281864730
23andMe allrs281864730
SNP Nexus

SNPshotrs281864730
SNPdbers281864730
MSV3drs281864730
GWAS Ctlgrs281864730
Max Magnitude0
ClinVar
Risk rs281864730(A,T;A,T)
Alt rs281864730(A,T;A,T)
Reference rs281864730(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910613C>A; NC_000006.11:g.29910613C>T
CLNSRC
CLNACC