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rs9391665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9391665(C;T)
Make rs9391665(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943529
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9391665
ebirs9391665
HLIrs9391665
Exacrs9391665
Varsomers9391665
Maprs9391665
PheGenIrs9391665
hapmaprs9391665
1000 genomesrs9391665
hgdprs9391665
ensemblrs9391665
gopubmedrs9391665
geneviewrs9391665
scholarrs9391665
googlers9391665
pharmgkbrs9391665
gwascentralrs9391665
openSNPrs9391665
23andMers9391665
23andMe allrs9391665
SNP Nexus

SNPshotrs9391665
SNPdbers9391665
MSV3drs9391665
GWAS Ctlgrs9391665
GMAF0.1405
Max Magnitude0
ClinVar
Risk rs9391665(G,T;G,T)
Alt rs9391665(G,T;G,T)
Reference rs9391665(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911306C>G; NC_000006.11:g.29911306C>T
CLNSRC
CLNACC