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rs267608259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs267608259(-;-)
Make rs267608259(-;GAA)
Make rs267608259(GAA;GAA)
ReferenceGRCh38 38.1/142
Chromosome6
Position83178682
GenePGM3
is asnp
is mentioned by
dbSNPrs267608259
ebirs267608259
HLIrs267608259
Exacrs267608259
Varsomers267608259
Maprs267608259
PheGenIrs267608259
hapmaprs267608259
1000 genomesrs267608259
hgdprs267608259
ensemblrs267608259
gopubmedrs267608259
geneviewrs267608259
scholarrs267608259
googlers267608259
pharmgkbrs267608259
gwascentralrs267608259
openSNPrs267608259
23andMers267608259
23andMe allrs267608259
SNP Nexus

SNPshotrs267608259
SNPdbers267608259
MSV3drs267608259
GWAS Ctlgrs267608259
Max Magnitude0
ClinVar
Risk rs267608259(;)
Alt rs267608259(;)
Reference rs267608259(AAG;AAG)
Significance Pathogenic
Disease Hyper-IgE syndrome
Variation info
Gene PGM3
CLNDBN Hyper-IgE syndrome
Reversed 1
HGVS NC_000006.11:g.83888401_83888403delTTC
CLNSRC ClinVar
CLNACC RCV000144535.1,