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rs79476640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs79476640(-;-)
Make rs79476640(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942960
GeneHLA-A
is asnp
is mentioned by
dbSNPrs79476640
ebirs79476640
HLIrs79476640
Exacrs79476640
Varsomers79476640
Maprs79476640
PheGenIrs79476640
hapmaprs79476640
1000 genomesrs79476640
hgdprs79476640
ensemblrs79476640
gopubmedrs79476640
geneviewrs79476640
scholarrs79476640
googlers79476640
pharmgkbrs79476640
gwascentralrs79476640
openSNPrs79476640
23andMers79476640
23andMe allrs79476640
SNP Nexus

SNPshotrs79476640
SNPdbers79476640
MSV3drs79476640
GWAS Ctlgrs79476640
Max Magnitude0
ClinVar
Risk rs79476640(;)
Alt rs79476640(;)
Reference rs79476640(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910737delG
CLNSRC
CLNACC