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rs937746465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position35860850
GeneIL7R, LOC105374724
is asnp
is mentioned by
dbSNPrs937746465
dbSNP (classic)rs937746465
ClinGenrs937746465
ebirs937746465
HLIrs937746465
Exacrs937746465
Gnomadrs937746465
Varsomers937746465
LitVarrs937746465
Maprs937746465
PheGenIrs937746465
Biobankrs937746465
1000 genomesrs937746465
hgdprs937746465
ensemblrs937746465
geneviewrs937746465
scholarrs937746465
googlers937746465
pharmgkbrs937746465
gwascentralrs937746465
openSNPrs937746465
23andMers937746465
SNPshotrs937746465
SNPdbers937746465
MSV3drs937746465
GWAS Ctlgrs937746465
Max Magnitude0
ClinVar
Risk rs937746465(T;T)
Alt rs937746465(T;T)
Reference Rs937746465(A;A)
Significance Pathogenic
Disease Severe Combined Immune Deficiency not provided
Variation info
Gene
CLNDBN Severe Combined Immune Deficiency not provided
Reversed 0
HGVS NC_000005.9:g.35860952A>T
CLNSRC
CLNACC RCV000341907.1, RCV000485322.1,