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rs193922642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922642(A;C)
Make rs193922642(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position35873481
GeneIL7R
is asnp
is mentioned by
dbSNPrs193922642
ebirs193922642
HLIrs193922642
Exacrs193922642
Varsomers193922642
Maprs193922642
PheGenIrs193922642
hapmaprs193922642
1000 genomesrs193922642
hgdprs193922642
ensemblrs193922642
gopubmedrs193922642
geneviewrs193922642
scholarrs193922642
googlers193922642
pharmgkbrs193922642
gwascentralrs193922642
openSNPrs193922642
23andMers193922642
23andMe allrs193922642
SNP Nexus

SNPshotrs193922642
SNPdbers193922642
MSV3drs193922642
GWAS Ctlgrs193922642
Max Magnitude0
ClinVar
Risk rs193922642(C;C)
Alt rs193922642(C;C)
Reference rs193922642(A;A)
Significance Probable-Pathogenic
Disease Severe combined immunodeficiency disease
Variation info
Gene IL7R
CLNDBN Severe combined immunodeficiency disease
Reversed 0
HGVS NC_000005.9:g.35873583A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030062.1,