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rs139910379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139910379(A;A)
Make rs139910379(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945108
GeneHLA-A
is asnp
is mentioned by
dbSNPrs139910379
ebirs139910379
HLIrs139910379
Exacrs139910379
Varsomers139910379
Maprs139910379
PheGenIrs139910379
hapmaprs139910379
1000 genomesrs139910379
hgdprs139910379
ensemblrs139910379
gopubmedrs139910379
geneviewrs139910379
scholarrs139910379
googlers139910379
pharmgkbrs139910379
gwascentralrs139910379
openSNPrs139910379
23andMers139910379
23andMe allrs139910379
SNP Nexus

SNPshotrs139910379
SNPdbers139910379
MSV3drs139910379
GWAS Ctlgrs139910379
GMAF0.1028
Max Magnitude0
ClinVar
Risk rs139910379(A;A)
Alt rs139910379(A;A)
Reference rs139910379(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912885C>A
CLNSRC
CLNACC