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rs1059896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059896(A;A)
Make rs1059896(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944565
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059896
dbSNP (classic)rs1059896
ClinGenrs1059896
ebirs1059896
HLIrs1059896
Exacrs1059896
Gnomadrs1059896
Varsomers1059896
LitVarrs1059896
Maprs1059896
PheGenIrs1059896
Biobankrs1059896
1000 genomesrs1059896
hgdprs1059896
ensemblrs1059896
geneviewrs1059896
scholarrs1059896
googlers1059896
pharmgkbrs1059896
gwascentralrs1059896
openSNPrs1059896
23andMers1059896
SNPshotrs1059896
SNPdbers1059896
MSV3drs1059896
GWAS Ctlgrs1059896
Max Magnitude0
ClinVar
Risk rs1059896(A;A)
Alt rs1059896(A;A)
Reference Rs1059896(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912342G>A
CLNSRC
CLNACC