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rs147423300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs147423300(A;A)
Make rs147423300(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position35860981
GeneIL7R, LOC105374724
is asnp
is mentioned by
dbSNPrs147423300
dbSNP (classic)rs147423300
ClinGenrs147423300
ebirs147423300
HLIrs147423300
Exacrs147423300
Gnomadrs147423300
Varsomers147423300
LitVarrs147423300
Maprs147423300
PheGenIrs147423300
Biobankrs147423300
1000 genomesrs147423300
hgdprs147423300
ensemblrs147423300
geneviewrs147423300
scholarrs147423300
googlers147423300
pharmgkbrs147423300
gwascentralrs147423300
openSNPrs147423300
23andMers147423300
SNPshotrs147423300
SNPdbers147423300
MSV3drs147423300
GWAS Ctlgrs147423300
Max Magnitude0
ClinVar
Risk rs147423300(A;A) rs147423300(C;C)
Alt rs147423300(A;A) rs147423300(C;C)
Reference Rs147423300(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL7R
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.35861083T>C
CLNSRC
CLNACC RCV000483484.1,