Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777565(C;C)
Make rs587777565(C;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position83171950
GenePGM3
is asnp
is mentioned by
dbSNPrs587777565
ebirs587777565
HLIrs587777565
Exacrs587777565
Varsomers587777565
Maprs587777565
PheGenIrs587777565
hapmaprs587777565
1000 genomesrs587777565
hgdprs587777565
ensemblrs587777565
gopubmedrs587777565
geneviewrs587777565
scholarrs587777565
googlers587777565
pharmgkbrs587777565
gwascentralrs587777565
openSNPrs587777565
23andMers587777565
23andMe allrs587777565
SNP Nexus

SNPshotrs587777565
SNPdbers587777565
MSV3drs587777565
GWAS Ctlgrs587777565
Max Magnitude0
ClinVar
Risk rs587777565(C,T;C,T)
Alt rs587777565(C,T;C,T)
Reference rs587777565(A;A)
Significance Pathogenic
Disease Immunodeficiency 23
Variation info
Gene PGM3
CLNDBN Immunodeficiency 23
Reversed 1
HGVS NC_000006.11:g.83881669T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000128847.4,