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rs28730670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28730670(C;T)
Make rs28730670(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position9717608
GenePIK3CD
is asnp
is mentioned by
dbSNPrs28730670
ebirs28730670
HLIrs28730670
Exacrs28730670
Varsomers28730670
Maprs28730670
PheGenIrs28730670
hapmaprs28730670
1000 genomesrs28730670
hgdprs28730670
ensemblrs28730670
gopubmedrs28730670
geneviewrs28730670
scholarrs28730670
googlers28730670
pharmgkbrs28730670
gwascentralrs28730670
openSNPrs28730670
23andMers28730670
23andMe allrs28730670
SNP Nexus

SNPshotrs28730670
SNPdbers28730670
MSV3drs28730670
GWAS Ctlgrs28730670
Max Magnitude0
ClinVar
Risk rs28730670(A,T;A,T)
Alt rs28730670(A,T;A,T)
Reference rs28730670(C;C)
Significance Pathogenic
Disease Immunodeficiency 14
Variation info
Gene PIK3CD
CLNDBN Immunodeficiency 14
Reversed 0
HGVS NC_000001.10:g.9777666C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000119275.3,