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rs786205646

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205646(-;-)
Make rs786205646(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position35875991
GeneIL7R
is asnp
is mentioned by
dbSNPrs786205646
ebirs786205646
HLIrs786205646
Exacrs786205646
Varsomers786205646
Maprs786205646
PheGenIrs786205646
hapmaprs786205646
1000 genomesrs786205646
hgdprs786205646
ensemblrs786205646
gopubmedrs786205646
geneviewrs786205646
scholarrs786205646
googlers786205646
pharmgkbrs786205646
gwascentralrs786205646
openSNPrs786205646
23andMers786205646
23andMe allrs786205646
SNP Nexus

SNPshotrs786205646
SNPdbers786205646
MSV3drs786205646
GWAS Ctlgrs786205646
Max Magnitude0
ClinVar
Risk rs786205646(;)
Alt rs786205646(;)
Reference rs786205646(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL7R
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.35876093delT
CLNSRC
CLNACC RCV000171518.1,