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rs80093308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80093308(C;C)
Make rs80093308(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356206
GeneHLA-B
is asnp
is mentioned by
dbSNPrs80093308
ebirs80093308
HLIrs80093308
Exacrs80093308
Varsomers80093308
Maprs80093308
PheGenIrs80093308
hapmaprs80093308
1000 genomesrs80093308
hgdprs80093308
ensemblrs80093308
gopubmedrs80093308
geneviewrs80093308
scholarrs80093308
googlers80093308
pharmgkbrs80093308
gwascentralrs80093308
openSNPrs80093308
23andMers80093308
23andMe allrs80093308
SNP Nexus

SNPshotrs80093308
SNPdbers80093308
MSV3drs80093308
GWAS Ctlgrs80093308
GMAF0.01699
Max Magnitude0
ClinVar
Risk rs80093308(C;C)
Alt rs80093308(C;C)
Reference rs80093308(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323983T>C
CLNSRC
CLNACC