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rs1057520377

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520377(A;G)
Make rs1057520377(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position42325013
GeneSTAT3
is asnp
is mentioned by
dbSNPrs1057520377
dbSNP (old)rs1057520377
ClinGenrs1057520377
ebirs1057520377
HLIrs1057520377
Exacrs1057520377
Gnomadrs1057520377
Varsomers1057520377
Maprs1057520377
PheGenIrs1057520377
Biobankrs1057520377
1000 genomesrs1057520377
hgdprs1057520377
ensemblrs1057520377
gopubmedrs1057520377
geneviewrs1057520377
scholarrs1057520377
googlers1057520377
pharmgkbrs1057520377
gwascentralrs1057520377
openSNPrs1057520377
23andMers1057520377
23andMe allrs1057520377
SNPshotrs1057520377
SNPdbers1057520377
MSV3drs1057520377
GWAS Ctlgrs1057520377
Max Magnitude0
ClinVar
Risk rs1057520377(G;G)
Alt rs1057520377(G;G)
Reference Rs1057520377(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STAT3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.40477031T>C
CLNSRC
CLNACC RCV000424764.1,