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rs769031989

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs769031989(A;A)
Make rs769031989(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position42322464
GeneSTAT3
is asnp
is mentioned by
dbSNPrs769031989
dbSNP (classic)rs769031989
ClinGenrs769031989
ebirs769031989
HLIrs769031989
Exacrs769031989
Gnomadrs769031989
Varsomers769031989
LitVarrs769031989
Maprs769031989
PheGenIrs769031989
Biobankrs769031989
1000 genomesrs769031989
hgdprs769031989
ensemblrs769031989
geneviewrs769031989
scholarrs769031989
googlers769031989
pharmgkbrs769031989
gwascentralrs769031989
openSNPrs769031989
23andMers769031989
SNPshotrs769031989
SNPdbers769031989
MSV3drs769031989
GWAS Ctlgrs769031989
Max Magnitude0
ClinVar
Risk rs769031989(A;A)
Alt rs769031989(A;A)
Reference Rs769031989(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.40474482T>A
CLNSRC
CLNACC RCV000414550.1,