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rs79566077

From SNPedia

Merged intors41548419
Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs79566077(-;-)
Make rs79566077(-;GAG)
Make rs79566077(GAG;GAG)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944452
GeneHLA-A
is asnp
is mentioned by
dbSNPrs79566077
ebirs79566077
HLIrs79566077
Exacrs79566077
Varsomers79566077
Maprs79566077
PheGenIrs79566077
hapmaprs79566077
1000 genomesrs79566077
hgdprs79566077
ensemblrs79566077
gopubmedrs79566077
geneviewrs79566077
scholarrs79566077
googlers79566077
pharmgkbrs79566077
gwascentralrs79566077
openSNPrs79566077
23andMers79566077
23andMe allrs79566077
SNP Nexus

SNPshotrs79566077
SNPdbers79566077
MSV3drs79566077
GWAS Ctlgrs79566077
StatusMerged into rs41548419
Max Magnitude0
ClinVar
Risk rs79566077(G,GGAG;G,GGAG)
Alt rs79566077(G,GGAG;G,GGAG)
Reference rs79566077(GG;GG)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912229delG
CLNSRC
CLNACC