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rs77467746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77467746(A;A)
Make rs77467746(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943827
GeneHLA-A
is asnp
is mentioned by
dbSNPrs77467746
ebirs77467746
HLIrs77467746
Exacrs77467746
Varsomers77467746
Maprs77467746
PheGenIrs77467746
hapmaprs77467746
1000 genomesrs77467746
hgdprs77467746
ensemblrs77467746
gopubmedrs77467746
geneviewrs77467746
scholarrs77467746
googlers77467746
pharmgkbrs77467746
gwascentralrs77467746
openSNPrs77467746
23andMers77467746
23andMe allrs77467746
SNP Nexus

SNPshotrs77467746
SNPdbers77467746
MSV3drs77467746
GWAS Ctlgrs77467746
Merged fromRs29028758
GMAF0.1579
Max Magnitude0
ClinVar
Risk rs77467746(A;A)
Alt rs77467746(A;A)
Reference rs77467746(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911604C>A
CLNSRC
CLNACC