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rs786205572

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205572(G;G)
Make rs786205572(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position35873578
GeneIL7R
is asnp
is mentioned by
dbSNPrs786205572
ebirs786205572
HLIrs786205572
Exacrs786205572
Varsomers786205572
Maprs786205572
PheGenIrs786205572
hapmaprs786205572
1000 genomesrs786205572
hgdprs786205572
ensemblrs786205572
gopubmedrs786205572
geneviewrs786205572
scholarrs786205572
googlers786205572
pharmgkbrs786205572
gwascentralrs786205572
openSNPrs786205572
23andMers786205572
23andMe allrs786205572
SNP Nexus

SNPshotrs786205572
SNPdbers786205572
MSV3drs786205572
GWAS Ctlgrs786205572
Max Magnitude0
ClinVar
Risk rs786205572(G;G)
Alt rs786205572(G;G)
Reference rs786205572(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL7R
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.35873680T>G
CLNSRC
CLNACC RCV000171382.1,