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rs1059537

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059537(G;T)
Make rs1059537(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943450
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059537
ebirs1059537
HLIrs1059537
Exacrs1059537
Varsomers1059537
Maprs1059537
PheGenIrs1059537
hapmaprs1059537
1000 genomesrs1059537
hgdprs1059537
ensemblrs1059537
gopubmedrs1059537
geneviewrs1059537
scholarrs1059537
googlers1059537
pharmgkbrs1059537
gwascentralrs1059537
openSNPrs1059537
23andMers1059537
23andMe allrs1059537
SNP Nexus

SNPshotrs1059537
SNPdbers1059537
MSV3drs1059537
GWAS Ctlgrs1059537
Max Magnitude0
ClinVar
Risk rs1059537(A,C,T;A,C,T)
Alt rs1059537(A,C,T;A,C,T)
Reference rs1059537(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911227G>A; NC_000006.11:g.29911227G>C; NC_000006.11:g.29911227G>T
CLNSRC
CLNACC