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rs79493767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs79493767(C;G)
Make rs79493767(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943273
GeneHLA-A
is asnp
is mentioned by
dbSNPrs79493767
ebirs79493767
HLIrs79493767
Exacrs79493767
Varsomers79493767
Maprs79493767
PheGenIrs79493767
hapmaprs79493767
1000 genomesrs79493767
hgdprs79493767
ensemblrs79493767
gopubmedrs79493767
geneviewrs79493767
scholarrs79493767
googlers79493767
pharmgkbrs79493767
gwascentralrs79493767
openSNPrs79493767
23andMers79493767
23andMe allrs79493767
SNP Nexus

SNPshotrs79493767
SNPdbers79493767
MSV3drs79493767
GWAS Ctlgrs79493767
Max Magnitude0
ClinVar
Risk rs79493767(G;G)
Alt rs79493767(G;G)
Reference rs79493767(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911050C>G
CLNSRC
CLNACC