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rs1064796922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position42322440
GeneSTAT3
is asnp
is mentioned by
dbSNPrs1064796922
dbSNP (classic)rs1064796922
ClinGenrs1064796922
ebirs1064796922
HLIrs1064796922
Exacrs1064796922
Gnomadrs1064796922
Varsomers1064796922
LitVarrs1064796922
Maprs1064796922
PheGenIrs1064796922
Biobankrs1064796922
1000 genomesrs1064796922
hgdprs1064796922
ensemblrs1064796922
geneviewrs1064796922
scholarrs1064796922
googlers1064796922
pharmgkbrs1064796922
gwascentralrs1064796922
openSNPrs1064796922
23andMers1064796922
SNPshotrs1064796922
SNPdbers1064796922
MSV3drs1064796922
GWAS Ctlgrs1064796922
Max Magnitude0
ClinVar
Risk rs1064796922(A;A)
Alt rs1064796922(A;A)
Reference Rs1064796922(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.40474458A>T
CLNSRC
CLNACC RCV000479714.1,