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rs77903928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77903928(C;T)
Make rs77903928(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943459
GeneHLA-A
is asnp
is mentioned by
dbSNPrs77903928
ebirs77903928
HLIrs77903928
Exacrs77903928
Varsomers77903928
Maprs77903928
PheGenIrs77903928
hapmaprs77903928
1000 genomesrs77903928
hgdprs77903928
ensemblrs77903928
gopubmedrs77903928
geneviewrs77903928
scholarrs77903928
googlers77903928
pharmgkbrs77903928
gwascentralrs77903928
openSNPrs77903928
23andMers77903928
23andMe allrs77903928
SNP Nexus

SNPshotrs77903928
SNPdbers77903928
MSV3drs77903928
GWAS Ctlgrs77903928
Max Magnitude0
ClinVar
Risk rs77903928(T;T)
Alt rs77903928(T;T)
Reference rs77903928(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911236C>T
CLNSRC
CLNACC