Have questions? Visit https://www.reddit.com/r/SNPedia

rs587778405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778405(G;T)
Make rs587778405(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position35873604
GeneIL7R
is asnp
is mentioned by
dbSNPrs587778405
dbSNP (classic)rs587778405
ClinGenrs587778405
ebirs587778405
HLIrs587778405
Exacrs587778405
Gnomadrs587778405
Varsomers587778405
LitVarrs587778405
Maprs587778405
PheGenIrs587778405
Biobankrs587778405
1000 genomesrs587778405
hgdprs587778405
ensemblrs587778405
geneviewrs587778405
scholarrs587778405
googlers587778405
pharmgkbrs587778405
gwascentralrs587778405
openSNPrs587778405
23andMers587778405
SNPshotrs587778405
SNPdbers587778405
MSV3drs587778405
GWAS Ctlgrs587778405
Max Magnitude0
ClinVar
Risk rs587778405(T;T)
Alt rs587778405(T;T)
Reference Rs587778405(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene IL7R
CLNDBN not specified not provided
Reversed 0
HGVS NC_000005.9:g.35873706G>T
CLNSRC
CLNACC RCV000121217.1, RCV000414042.1,