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rs397518423

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397518423(A;A)
Make rs397518423(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position9726972
GenePIK3CD
is asnp
is mentioned by
dbSNPrs397518423
ebirs397518423
HLIrs397518423
Exacrs397518423
Varsomers397518423
Maprs397518423
PheGenIrs397518423
hapmaprs397518423
1000 genomesrs397518423
hgdprs397518423
ensemblrs397518423
gopubmedrs397518423
geneviewrs397518423
scholarrs397518423
googlers397518423
pharmgkbrs397518423
gwascentralrs397518423
openSNPrs397518423
23andMers397518423
23andMe allrs397518423
SNP Nexus

SNPshotrs397518423
SNPdbers397518423
MSV3drs397518423
GWAS Ctlgrs397518423
Max Magnitude0
ClinVar
Risk rs397518423(A;A)
Alt rs397518423(A;A)
Reference rs397518423(G;G)
Significance Pathogenic
Disease Immunodeficiency 14 not provided
Variation info
Gene PIK3CD
CLNDBN Immunodeficiency 14 not provided
Reversed 0
HGVS NC_000001.10:g.9787030G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000076908.6, RCV000224521.1,