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rs193922644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922644(A;A)
Make rs193922644(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position35873559
GeneIL7R
is asnp
is mentioned by
dbSNPrs193922644
ebirs193922644
HLIrs193922644
Exacrs193922644
Varsomers193922644
Maprs193922644
PheGenIrs193922644
hapmaprs193922644
1000 genomesrs193922644
hgdprs193922644
ensemblrs193922644
gopubmedrs193922644
geneviewrs193922644
scholarrs193922644
googlers193922644
pharmgkbrs193922644
gwascentralrs193922644
openSNPrs193922644
23andMers193922644
23andMe allrs193922644
SNP Nexus

SNPshotrs193922644
SNPdbers193922644
MSV3drs193922644
GWAS Ctlgrs193922644
Max Magnitude0
ClinVar
Risk rs193922644(A,T;A,T)
Alt rs193922644(A,T;A,T)
Reference rs193922644(G;G)
Significance Probable-Pathogenic
Disease Severe combined immunodeficiency disease
Variation info
Gene IL7R
CLNDBN Severe combined immunodeficiency disease
Reversed 0
HGVS NC_000005.9:g.35873661G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030064.1,