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rs1057521091

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521091(A;C)
Make rs1057521091(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position42325030
GeneSTAT3
is asnp
is mentioned by
dbSNPrs1057521091
dbSNP (old)rs1057521091
ClinGenrs1057521091
ebirs1057521091
HLIrs1057521091
Exacrs1057521091
Gnomadrs1057521091
Varsomers1057521091
Maprs1057521091
PheGenIrs1057521091
Biobankrs1057521091
1000 genomesrs1057521091
hgdprs1057521091
ensemblrs1057521091
gopubmedrs1057521091
geneviewrs1057521091
scholarrs1057521091
googlers1057521091
pharmgkbrs1057521091
gwascentralrs1057521091
openSNPrs1057521091
23andMers1057521091
23andMe allrs1057521091
SNPshotrs1057521091
SNPdbers1057521091
MSV3drs1057521091
GWAS Ctlgrs1057521091
Max Magnitude0
ClinVar
Risk rs1057521091(C;C) rs1057521091(G;G)
Alt rs1057521091(C;C) rs1057521091(G;G)
Reference Rs1057521091(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.40477048T>C; NC_000017.10:g.40477048T>G
CLNSRC
CLNACC RCV000486952.1, RCV000417632.1,