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rs56343262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56343262(A;A)
Make rs56343262(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943303
GeneHLA-A
is asnp
is mentioned by
dbSNPrs56343262
ebirs56343262
HLIrs56343262
Exacrs56343262
Varsomers56343262
Maprs56343262
PheGenIrs56343262
hapmaprs56343262
1000 genomesrs56343262
hgdprs56343262
ensemblrs56343262
gopubmedrs56343262
geneviewrs56343262
scholarrs56343262
googlers56343262
pharmgkbrs56343262
gwascentralrs56343262
openSNPrs56343262
23andMers56343262
23andMe allrs56343262
SNP Nexus

SNPshotrs56343262
SNPdbers56343262
MSV3drs56343262
GWAS Ctlgrs56343262
Max Magnitude0
ClinVar
Risk rs56343262(A,C,T;A,C,T)
Alt rs56343262(A,C,T;A,C,T)
Reference rs56343262(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911080G>A; NC_000006.11:g.29911080G>C; NC_000006.11:g.29911080G>T
CLNSRC
CLNACC