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rs200044623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200044623(G;G)
Make rs200044623(G;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position35860992
GeneIL7R, LOC105374724
is asnp
is mentioned by
dbSNPrs200044623
dbSNP (classic)rs200044623
ClinGenrs200044623
ebirs200044623
HLIrs200044623
Exacrs200044623
Gnomadrs200044623
Varsomers200044623
LitVarrs200044623
Maprs200044623
PheGenIrs200044623
Biobankrs200044623
1000 genomesrs200044623
hgdprs200044623
ensemblrs200044623
geneviewrs200044623
scholarrs200044623
googlers200044623
pharmgkbrs200044623
gwascentralrs200044623
openSNPrs200044623
23andMers200044623
SNPshotrs200044623
SNPdbers200044623
MSV3drs200044623
GWAS Ctlgrs200044623
Max Magnitude0
ClinVar
Risk rs200044623(G;G)
Alt rs200044623(G;G)
Reference Rs200044623(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene IL7R
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.35861094T>G
CLNSRC
CLNACC RCV000255196.1,