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rs587777564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777564(-;-)
Make rs587777564(-;T)
Make rs587777564(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position83181786
GenePGM3
is asnp
is mentioned by
dbSNPrs587777564
ebirs587777564
HLIrs587777564
Exacrs587777564
Varsomers587777564
Maprs587777564
PheGenIrs587777564
hapmaprs587777564
1000 genomesrs587777564
hgdprs587777564
ensemblrs587777564
gopubmedrs587777564
geneviewrs587777564
scholarrs587777564
googlers587777564
pharmgkbrs587777564
gwascentralrs587777564
openSNPrs587777564
23andMers587777564
23andMe allrs587777564
SNP Nexus

SNPshotrs587777564
SNPdbers587777564
MSV3drs587777564
GWAS Ctlgrs587777564
Max Magnitude0
ClinVar
Risk rs587777564(T;T)
Alt rs587777564(T;T)
Reference rs587777564(;)
Significance Pathogenic
Disease Immunodeficiency 23
Variation info
Gene PGM3
CLNDBN Immunodeficiency 23
Reversed 0
HGVS NC_000006.11:g.83891505dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000128846.4,