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rs587777389

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777389(A;A)
Make rs587777389(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position9720793
GenePIK3CD
is asnp
is mentioned by
dbSNPrs587777389
ebirs587777389
HLIrs587777389
Exacrs587777389
Varsomers587777389
Maprs587777389
PheGenIrs587777389
hapmaprs587777389
1000 genomesrs587777389
hgdprs587777389
ensemblrs587777389
gopubmedrs587777389
geneviewrs587777389
scholarrs587777389
googlers587777389
pharmgkbrs587777389
gwascentralrs587777389
openSNPrs587777389
23andMers587777389
23andMe allrs587777389
SNP Nexus

SNPshotrs587777389
SNPdbers587777389
MSV3drs587777389
GWAS Ctlgrs587777389
Max Magnitude0
ClinVar
Risk rs587777389(A;A)
Alt rs587777389(A;A)
Reference rs587777389(G;G)
Significance Pathogenic
Disease Immunodeficiency 14
Variation info
Gene PIK3CD
CLNDBN Immunodeficiency 14
Reversed 0
HGVS NC_000001.10:g.9780851G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000119276.3,