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rs1064794957

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position42317182
GeneSTAT3
is asnp
is mentioned by
dbSNPrs1064794957
dbSNP (classic)rs1064794957
ClinGenrs1064794957
ebirs1064794957
HLIrs1064794957
Exacrs1064794957
Gnomadrs1064794957
Varsomers1064794957
LitVarrs1064794957
Maprs1064794957
PheGenIrs1064794957
Biobankrs1064794957
1000 genomesrs1064794957
hgdprs1064794957
ensemblrs1064794957
geneviewrs1064794957
scholarrs1064794957
googlers1064794957
pharmgkbrs1064794957
gwascentralrs1064794957
openSNPrs1064794957
23andMers1064794957
SNPshotrs1064794957
SNPdbers1064794957
MSV3drs1064794957
GWAS Ctlgrs1064794957
Max Magnitude0
ClinVar
Risk rs1064794957(T;T)
Alt rs1064794957(T;T)
Reference Rs1064794957(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.40469200G>A
CLNSRC
CLNACC RCV000482055.1,